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<title>Preventive and Behavioral Medicine Publications and Presentations</title>
<copyright>Copyright (c) 2013 University of Massachusetts Medical School All rights reserved.</copyright>
<link>http://escholarship.umassmed.edu/prevbeh_pp</link>
<description>Recent documents in Preventive and Behavioral Medicine Publications and Presentations</description>
<language>en-us</language>
<lastBuildDate>Fri, 17 May 2013 11:55:09 PDT</lastBuildDate>
<ttl>3600</ttl>








<item>
<title>The Adoption and Spread of a Core-Strengthening Exercise Through an Online Social Network</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/264</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/264</guid>
<pubDate>Tue, 26 Feb 2013 08:46:52 PST</pubDate>
<description>
	<![CDATA[
	<p><strong>BACKGROUND:</strong></p>
<p>The present feasibility study describes engagement and spread of a Twitter-based core-strengthening challenge.</p>
<p><strong>METHODS:</strong></p>
<p>A challenge that entailed completing a core-strengthening exercise using a hashtag (<a href="http://www.ncbi.nlm.nih.gov/pubmed/?term=23416874#">#PlankADay</a>) was circulated via Twitter. We surveyed users who joined during the first 2 months of the challenge to describe their characteristics, including social support for exercise and to what extent they invited others to join. We continued to track total users for 10 months.</p>
<p><strong>RESULTS:</strong></p>
<p>Of 407 individuals who joined in the first 2 months, 105 completed surveys. Among these, 81% were female and 86% Caucasian and mean age was 35.8. 72% participated for at least 1 month and 47% participated for at least 2 months. Survey participants reported that the challenge increased their enjoyment of abdominal exercise. Of the 68% of participants who invited others to participate, 28% recruited none, 66% recruited 1-5 users, and 6% recruited 10 or more users. Participants reported that online friends provided as much positive social support for exercise as family and in-person friends. In 14 months, 4,941 users produced 76,746 tweets and mean total tweets per user was 15.86 (SD = 75.34; range= 1-2888).</p>
<p><strong>CONCLUSION:</strong></p>
<p>Online social networks may be a promising mechanism to spread brief exercise behaviors.</p>

	]]>
</description>

<author>Sherry L. Pagoto et al.</author>


<category>Muscle Strength</category>

<category>Exercise</category>

<category>Physical Fitness</category>

<category>Health Behavior</category>

<category>Social Networking</category>

<category>Internet</category>

</item>






<item>
<title>Antidepressant Use, Depression, and New Onset Diabetes among Elderly Medicare Beneficiaries</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/262</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/262</guid>
<pubDate>Fri, 18 Jan 2013 07:38:26 PST</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVE: To examine the association between antidepressant use, diagnosed depression, and new onset diabetes among elderly Medicare beneficiaries.</p>
<p>MATERIALS AND METHODS: Longitudinal data from merged survey and claims from the nationally representative Medicare Current Beneficiary Survey(MCBS) from 1999-2005 were used. Diabetes incidence was extracted from claims and survey data over a 3-year period. Depression and antidepressant use data were obtained over time. Multivariable logistic regressions were used to examine association between antidepressant use, depression, and new onset diabetes, adjusted for demographic, socioeconomic, and lifestyle risk factors. Analyses accounted for complex design of MCBS.</p>
<p>RESULTS: Incident diabetes rate was 4.8% for those "without depression and without antidepressants" and 9.5% for those with any antidepressant use in all 3-years and diagnosed depression. Compared to Medicare beneficiaries who did not report any antidepressant use, beneficiaries reporting antidepressant use in all 3-years were 50% more likely to have new onset diabetes. However, when diagnosed depression was entered in the model, we did not observe a statistically significant association between long-term antidepressant use and new onset diabetes. Medicare beneficiaries with any depression were twice as likely as those without depression to develop diabetes(AOR = 2.04, [1.51, 2.75).</p>
<p>CONCLUSION: Depression could independently increase risk of developing diabetes, while there is no evidence of association between antidepressants and new onset diabetes. If replicated, these results have significant clinical implications.</p>
<p>THE SIGNIFICANT FINDING OF THE STUDY: We found increased diabetes risk among Medicare beneficiaries with depression.</p>
<p>THIS STUDY ADDS: Long-term use of antidepressants in the absence of depression increases risk of diabetes.</p>

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</description>

<author>Usha Sambamoorthi et al.</author>


<category>Antidepressive Agents</category>

<category>Depression</category>

<category>Diabetes Mellitus, Type 2</category>

<category>Medicare</category>

</item>






<item>
<title>Statin therapy and the risk for diabetes among adult women: do the benefits outweigh the risk</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/261</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/261</guid>
<pubDate>Fri, 18 Jan 2013 07:38:25 PST</pubDate>
<description>
	<![CDATA[
	<p>Purpose of review: The purpose of this review was to examine statin therapy and the risk for diabetes among adult women using a selective review.</p>
<p>Recent findings: The literature contains reports of new-onset diabetes associated with statin use. While many studies do not report sex-specific results, there is evidence indicating the risk to benefit ratio may vary by gender. However, the absolute effects are not clear because women have historically been under-represented in clinical trials.</p>
<p>Summary: A review of the literature indicates that the cardiovascular benefits of statins appear to outweigh the risk for statin-related diabetes. However, the effect may depend upon baseline diabetes risk, dose, and statin potency. Rigorous, long-term studies focused on the risks and benefits of statins in women are unavailable to sort for gender-specific differences. Until this changes, individualized attention to risk assessment, and strong prevention with lifestyle changes must prevail.</p>

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</description>

<author>Yunsheng Ma et al.</author>


<category>Diabetes Mellitus, Type 2</category>

<category>Hydroxymethylglutaryl-CoA Reductase Inhibitors</category>

</item>






<item>
<title>Validity of self-reported height and weight and factors associated with errors in self-report</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/263</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/263</guid>
<pubDate>Fri, 18 Jan 2013 07:31:28 PST</pubDate>
<description>
	<![CDATA[
	<p>The aim of this investigation is to assess the validity of self-reported height and weight and to examine factors associated with errors in self-report. A cross-sectional study was conducted in Coimbatore, Tamil Nadu, South India, from June 20 to August 20, 2011. The study involved 389 men and 355 women aged 20 years and above. We found that self-reported height and weight were significantly correlated with measured height and weight for men and women [Pearson’s correlation coefficient(r) for men and women: 0.61 and 0.44 in height, 0.91 and 0.85 in weight, 0.76 and 0.64 in body mass index (BMI), respectively]. The prevalence of obesity based on self-reported height and weight were 7.9 and 15.8% for men and women, respectively, which was slightly smaller than that based on measured data 7.7 and 19.7%, respectively. Sensitivity and specificity of obesity based on self-report for both men and women were 97, 62% in men and 89, 64% in women, respectively. Participants with higher measured BMI significantly underestimated their weight compared to those with smaller BMI. It is also observed that among both men and women with measured BMI above 18.5 kg/m<sup>2</sup> were likely to underestimate their weight and BMI below 18.5 kg/m<sup>2</sup>were likely to overestimate their weight. However, the presence of diabetes, hypertension and heart disease was not associated with the difference between measured and self-reported height and weight for both men and women. Our findings indicate that self-reported weight has an acceptable agreement with measured data, but self-reported height has only a moderate agreement with measured data. There were no significant differences by presence of chronic disease and educational level between the self-reported and measured height and weight in both men and women.</p>

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</description>

<author>Anil Chankaramangalam Mathew et al.</author>


<category>Body Weight</category>

<category>Body Height</category>

<category>Self Report</category>

<category>Reproducibility of Results</category>

</item>






<item>
<title>Effect of Paget&apos;s disease on survival in breast cancer: an exploratory study</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/260</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/260</guid>
<pubDate>Wed, 14 Nov 2012 12:33:52 PST</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVE: To explore whether Paget's disease (PD) has an effect on outcome in patients with breast cancer.</p>
<p>DESIGN: Retrospective analysis of comprehensive pathology database, medical records, and slides of samples showing pathologic features.</p>
<p>SETTING: UMass Memorial Health Care.</p>
<p>PATIENTS: All patients with breast cancer and PD with records in a prospectively maintained database between January 1, 1990, and December 31, 2008, were identified. Each participant was matched (criteria: age within 5 years, year of treatment, and stage of breast cancer) with 2 controls (1:2 ratio).</p>
<p>MAIN OUTCOME MEASURES: Overall and disease-free survival were analyzed using Kaplan-Meier statistics and Cox proportional hazards modeling, accounting for matching in the latter analyses by using robust standard error estimates.</p>
<p>RESULTS: Mean (SD) follow-up was 47 (33) months. Treatment involved mastectomy in 29 (91%) PD vs 16 (25%) non-PD patients (P < .001), radiotherapy in 14 (44%) PD vs 53 (83%) non-PD patients (P < .001), and hormonal therapy in 14 (44%) PD vs 33 (52%) non-PD patients (P = .004). Biological markers were not significantly different except for ERBB2 (formerly HER2 or HER2/neu) overexpression in 14 (44%) PD vs 16 (25%) non-PD patients (P = .008). The PD group had an overall 5-year survival of 81.2% vs 93.8% of the non-PD group (Kaplan-Meier log-rank, P = .03). The unadjusted hazard ratio for the PD vs non-PD group was 5.31 (95% CI, 1.74-16.27; P = .003). The corresponding hazard ratio after adjusting for local and systemic treatment was 2.26 (95% CI, 0.46-11.06; P = .32).</p>
<p>CONCLUSIONS: These exploratory data show that PD may have a negative effect on breast cancer survival. This finding needs to be substantiated in larger data sets.</p>

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</description>

<author>Sonia Ortiz-Pagan et al.</author>


<category>Breast Neoplasms</category>

<category>Disease-Free Survival</category>

<category>Female</category>

<category>Follow-Up Studies</category>

<category>Humans</category>

<category>Massachusetts</category>

<category>Middle Aged</category>

<category>Neoplasm Staging</category>

<category>Paget&apos;s Disease, Mammary</category>

<category>Prognosis</category>

<category>Retrospective Studies</category>

<category>Risk Factors</category>

<category>*SEER Program</category>

<category>Survival Rate</category>

</item>






<item>
<title>Indoor and outdoor falls in older adults are different: the maintenance of balance, independent living, intellect, and Zest in the Elderly of Boston Study</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/259</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/259</guid>
<pubDate>Wed, 14 Nov 2012 12:33:51 PST</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVES: To identify risk factors for indoor and outdoor falls.</p>
<p>DESIGN: Prospective cohort study.</p>
<p>SETTING: The MOBILIZE Boston Study, a study of falls etiology in community-dwelling older individuals.</p>
<p>PARTICIPANTS: Seven hundred sixty-five women and men, mainly aged 70 and older, from randomly sampled households in the Boston, Massachusetts, area.</p>
<p>MEASUREMENTS: Baseline data were collected by questionnaire and comprehensive clinic examination. During follow-up, participants recorded falls on daily calendars. The location and circumstances of each fall were asked during telephone interviews.</p>
<p>RESULTS: Five hundred ninety-eight indoor and 524 outdoor falls were reported over a median follow-up of 21.7 months. Risk factors for indoor falls included older age, being female, and various indicators of poor health. Risk factors for outdoor falls included younger age, being male, and being relatively physically active and healthy. For instance, the age- and sex-adjusted rate ratio for having much difficulty or inability to perform activities of daily living relative to no difficulty was 2.57 (95% confidence interval (CI) = 1.69-3.90) for indoor falls but 0.27 (95% CI = 0.13-0.56) for outdoor falls. The rate ratio for gait speed of less than 0.68 m/s relative to a speed of greater than 1.33 m/s was 1.48 (95% CI = 0.81-2.68) for indoor falls but 0.27 (95% CI = 0.15-0.50) for outdoor falls.</p>
<p>CONCLUSION: Risk factors for indoor and outdoor falls differ. Combining these falls, as is done in many studies, masks important information. Prevention recommendations for noninstitutionalized older people would probably be more effective if targeted differently for frail, inactive older people at high risk for indoor falls and relatively active, healthy people at high risk for outdoor falls. Geriatrics Society.</p>

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</description>

<author>Jennifer L. Kelsey et al.</author>


<category>Accidental Falls</category>

<category>Accidents, Home</category>

<category>Aged</category>

<category>Aged, 80 and over</category>

<category>Female</category>

<category>Humans</category>

<category>*Independent Living</category>

<category>*Intelligence</category>

<category>Male</category>

<category>Middle Aged</category>

<category>*Postural Balance</category>

<category>Prospective Studies</category>

<category>Risk Factors</category>

</item>






<item>
<title>Movement Disorder Society-sponsored revision of the Unified Parkinson&apos;s Disease Rating Scale (MDS-UPDRS): Process, format, and clinimetric testing plan</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/258</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/258</guid>
<pubDate>Thu, 25 Oct 2012 11:13:24 PDT</pubDate>
<description>
	<![CDATA[
	<p>This article presents the revision process, major innovations, and clinimetric testing program for the Movement Disorder Society (MDS)-sponsored revision of the Unified Parkinson's Disease Rating Scale (UPDRS), known as the MDS-UPDRS. The UPDRS is the most widely used scale for the clinical study of Parkinson's disease (PD). The MDS previously organized a critique of the UPDRS, which cited many strengths, but recommended revision of the scale to accommodate new advances and to resolve problematic areas. An MDS-UPDRS committee prepared the revision using the recommendations of the published critique of the scale. Subcommittees developed new material that was reviewed by the entire committee. A 1-day face-to-face committee meeting was organized to resolve areas of debate and to arrive at a working draft ready for clinimetric testing. The MDS-UPDRS retains the UPDRS structure of four parts with a total summed score, but the parts have been modified to provide a section that integrates nonmotor elements of PD: I, Nonmotor Experiences of Daily Living; II, Motor Experiences of Daily Living; III, Motor Examination; and IV, Motor Complications. All items have five response options with uniform anchors of 0 = normal, 1 = slight, 2 = mild, 3 = moderate, and 4 = severe. Several questions in Part I and all of Part II are written as a patient/caregiver questionnaire, so that the total rater time should remain approximately 30 minutes. Detailed instructions for testing and data acquisition accompany the MDS-UPDRS in order to increase uniform usage. Multiple language editions are planned. A three-part clinimetric program will provide testing of reliability, validity, and responsiveness to interventions. Although the MDS-UPDRS will not be published until it has successfully passed clinimetric testing, explanation of the process, key changes, and clinimetric programs allow clinicians and researchers to understand and participate in the revision process.</p>

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</description>

<author>Christopher Goetz et al.</author>


<category>*Disability Evaluation</category>

<category>Humans</category>

<category>Movement Disorders</category>

<category>Parkinson Disease</category>

<category>*Psychometrics</category>

<category>Questionnaires</category>

<category>Reproducibility of Results</category>

<category>Severity of Illness Index</category>

</item>






<item>
<title>Movement Disorder Society-sponsored revision of the Unified Parkinson&apos;s Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing results</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/257</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/257</guid>
<pubDate>Thu, 25 Oct 2012 11:13:22 PDT</pubDate>
<description>
	<![CDATA[
	<p>We present a clinimetric assessment of the Movement Disorder Society (MDS)-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS). The MDS-UDPRS Task Force revised and expanded the UPDRS using recommendations from a published critique. The MDS-UPDRS has four parts, namely, I: Non-motor Experiences of Daily Living; II: Motor Experiences of Daily Living; III: Motor Examination; IV: Motor Complications. Twenty questions are completed by the patient/caregiver. Item-specific instructions and an appendix of complementary additional scales are provided. Movement disorder specialists and study coordinators administered the UPDRS (55 items) and MDS-UPDRS (65 items) to 877 English speaking (78% non-Latino Caucasian) patients with Parkinson's disease from 39 sites. We compared the two scales using correlative techniques and factor analysis. The MDS-UPDRS showed high internal consistency (Cronbach's alpha = 0.79-0.93 across parts) and correlated with the original UPDRS (rho = 0.96). MDS-UPDRS across-part correlations ranged from 0.22 to 0.66. Reliable factor structures for each part were obtained (comparative fit index > 0.90 for each part), which support the use of sum scores for each part in preference to a total score of all parts. The combined clinimetric results of this study support the validity of the MDS-UPDRS for rating PD.</p>

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</description>

<author>Christopher Goetz et al.</author>


<category>Adult</category>

<category>Aged</category>

<category>Aged, 80 and over</category>

<category>*Disability Evaluation</category>

<category>Factor Analysis, Statistical</category>

<category>Female</category>

<category>Humans</category>

<category>Male</category>

<category>Middle Aged</category>

<category>Movement Disorders</category>

<category>Neurologic Examination</category>

<category>Parkinson Disease</category>

<category>*Severity of Illness Index</category>

<category>Societies, Medical</category>

</item>






<item>
<title>Exploratory research to design a school nurse-delivered intervention to treat adolescent overweight and obesity</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/256</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/256</guid>
<pubDate>Thu, 25 Oct 2012 11:13:21 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVE: In preparation for a pilot study to evaluate the efficacy of a school nurse-delivered intervention, focus groups were conducted to gain insight into the perceptions of stakeholders regarding the design and implementation of the intervention.</p>
<p>SETTING AND PARTICIPANTS: Fifteen focus groups at participating schools. One hundred subjects, including overweight and obese high school students, parents, high school nurses, and staff.</p>
<p>MAIN OUTCOME MEASURE: Stakeholders' perceptions.</p>
<p>ANALYSIS: Focus groups were audiotaped and transcribed verbatim. Theme instances related to the research aim were identified, coded, and sorted into theme categories.</p>
<p>RESULTS: Major topics discussed included teen issues, family support, intervention implementation-related concerns, and curriculum content. Teen issues included dealing with peer pressure, avoiding emotional eating, and support from friends. Many participants thought it should be the teen's choice to involve parents. Confidentiality was the most commonly identified potential barrier to implementation. Recommendations for nutrition and physical activity curriculum content focused on concrete, practical strategies.</p>
<p>CONCLUSIONS AND IMPLICATIONS: Results of this research provided insight into stakeholder's needs and perceptions regarding the content and structure of a school nurse-delivered intervention to treat adolescent overweight and obesity. Findings were used in the design and implementation of intervention protocols and materials. Elsevier Inc. All rights reserved.</p>

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</description>

<author>Lauren A. Gellar et al.</author>


<category>Adolescent</category>

<category>Adult</category>

<category>Female</category>

<category>Focus Groups</category>

<category>Food Habits</category>

<category>Health Promotion</category>

<category>Humans</category>

<category>Male</category>

<category>Middle Aged</category>

<category>Obesity</category>

<category>Overweight</category>

<category>Parents</category>

<category>School Nursing</category>

<category>Social Behavior</category>

</item>






<item>
<title>Effect of mindfulness training on asthma quality of life and lung function: a randomised controlled trial</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/255</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/255</guid>
<pubDate>Thu, 25 Oct 2012 11:13:20 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: This study evaluated the efficacy of a mindfulness training programme (mindfulness-based stress reduction (MBSR)) in improving asthma-related quality of life and lung function in patients with asthma.</p>
<p>METHODS: A randomised controlled trial compared an 8-week MBSR group-based programme (n=42) with an educational control programme (n=41) in adults with mild, moderate or severe persistent asthma recruited at a university hospital outpatient primary care and pulmonary care clinic. Primary outcomes were quality of life (Asthma Quality of Life Questionnaire) and lung function (change from baseline in 2-week average morning peak expiratory flow (PEF)). Secondary outcomes were asthma control assessed by 2007 National Institutes of Health/National Heart Lung and Blood Institute guidelines, and stress (Perceived Stress Scale (PSS)). Follow-up assessments were conducted at 10 weeks, 6 and 12 months.</p>
<p>RESULTS: At 12 months MBSR resulted in clinically significant improvements from baseline in quality of life (differential change in Asthma Quality of Life Questionnaire score for MBSR vs control: 0.66 (95% CI 0.30 to 1.03; p<0.001)) but not in lung function (morning PEF, PEF variability and forced expiratory volume in 1 s). MBSR also resulted in clinically significant improvements in perceived stress (differential change in PSS score for MBSR vs control: -4.5 (95% CI -7.1 to -1.9; p=0.001)). There was no significant difference (p=0.301) in percentage of patients in MBSR with well controlled asthma (7.3% at baseline to 19.4%) compared with the control condition (7.5% at baseline to 7.9%).</p>
<p>CONCLUSIONS: MBSR produced lasting and clinically significant improvements in asthma-related quality of life and stress in patients with persistent asthma, without improvements in lung function.</p>
<p>CLINICAL TRIAL REGISTRATION NUMBER: Asthma and Mindfulness-Based Reduction (MBSR) Identifier: NCT00682669. clinicaltrials.gov.</p>

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</description>

<author>Lori Pbert et al.</author>


<category>Asthma</category>

<category>Meditation</category>

<category>Quality of Life</category>

<category>Stress, Psychological</category>

</item>






<item>
<title>Development and validation of worksite weight-related social norms surveys</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/254</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/254</guid>
<pubDate>Thu, 25 Oct 2012 11:13:19 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVE: To describe the development of measures of worksite descriptive social norms for weight loss, physical activity, and eating behaviors.</p>
<p>METHODS: Three surveys were tested in 844 public high school employees. Factor analysis, Cronbach alpha, and tests of association with other worksite social contextual measures and behaviors were performed.</p>
<p>RESULTS: Each survey demonstrated high internal consistency and was associated with measures of social support and behaviors. Confirmatory factor analysis supported the reliability of the weight-loss and eating-behavior norms surveys, but not the physical-activity norms survey.</p>
<p>CONCLUSIONS: The weight-loss and eating norms surveys are reliable, valid measures.</p>

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</description>

<author>Stephenie C. Lemon et al.</author>


<category>Data Collection</category>

<category>Weight Loss</category>

<category>Motor Activity</category>

<category>Feeding Behavior</category>

<category>Workplace</category>

<category>Health Surveys</category>

</item>






<item>
<title>Male inclusion in randomized controlled trials of lifestyle weight loss interventions</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/253</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/253</guid>
<pubDate>Thu, 25 Oct 2012 11:13:18 PDT</pubDate>
<description>
	<![CDATA[
	<p>The prevalence of obesity is similar for men (32.2%) and women (35.5%). It has been assumed that lifestyle weight loss interventions have been developed and tested in predominately female samples, but this has not been systematically investigated. The aim of this review was to investigate total and ethnic male inclusion in randomized controlled trials of lifestyle interventions. PUBMED, MEDLINE, and PSYCHINFO were searched for randomized controlled trials of lifestyle weight loss interventions (N = 244 studies with a total of 95,207 participants) published in the last 10 years (1999-2009). A trial must be in English, included weight loss as an outcome, and tested a dietary, exercise, and/or other behavioral intervention for weight loss. Results revealed samples were on average 27% male vs. 73% female (P < 0.001). Trials recruiting a diseased sample included a larger proportion of males than those not targeting a disease (35% vs. 21%; P < 0.001). About 32% of trials used exclusively female samples, whereas only 5% used exclusively male samples (P < 0.001). No studies in the past 10 years specifically targeted minority males. Ethnic males identified composed 1.8% of total participants in US studies. Only 24% of studies that underrepresented males provided a reason. Males, especially ethnic males, are underrepresented in lifestyle weight loss trials.</p>

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</description>

<author>Sherry L. Pagoto et al.</author>


<category>Ethnic Groups</category>

<category>Female</category>

<category>Humans</category>

<category>Male</category>

<category>*Men&apos;s Health</category>

<category>Obesity</category>

<category>Randomized Controlled Trials as Topic</category>

<category>*Risk Reduction Behavior</category>

<category>United States</category>

<category>*Weight Loss</category>

</item>






<item>
<title>The emotional eating scale. Can a self-report measure predict observed emotional eating</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/252</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/252</guid>
<pubDate>Thu, 25 Oct 2012 11:13:17 PDT</pubDate>
<description>
	<![CDATA[
	<p>We assessed the validity of the emotional eating scale (EES) by examining whether the EES predicted food intake following two negative mood inductions. Participants underwent mood inductions for anxiety, anger and neutral mood, then received snack foods in a sham palatability test. EES anxiety, but not anger, predicted intake. Participants high on EES anxiety consumed more snacks during the anxiety mood induction, whereas participants low on EES anxiety consumed less snacks. Results suggest that EES anxiety is a predictor of anxiety-driven eating and may be used to assess emotional eating when direct observation of intake is not possible.</p>

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</description>

<author>Kristin L. Schneider et al.</author>


<category>Adult</category>

<category>Affect</category>

<category>Anger</category>

<category>Anxiety</category>

<category>Eating</category>

<category>*Emotions</category>

<category>Feeding Behavior</category>

<category>Female</category>

<category>Humans</category>

<category>Male</category>

<category>Questionnaires</category>

<category>Reproducibility of Results</category>

<category>Self Report</category>

</item>






<item>
<title>Delay discounting and intake of ready-to-eat and away-from-home foods in overweight and obese women</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/250</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/250</guid>
<pubDate>Thu, 25 Oct 2012 11:13:16 PDT</pubDate>
<description>
	<![CDATA[
	<p>A shift from home-prepared to away-from-home and ready-to-eat foods has occurred in recent decades, which has implications for obesity and health. This study tested whether delay discounting, a facet of impulsivity reflecting sensitivity to immediate reward, is associated with the frequency of consumption and typical amount consumed of home-prepared, away-from-home, and ready-to-eat foods among overweight and obese women. Seventy-eight participants completed a binary choice task assessing discounting of delayed monetary rewards. Nutrient analysis of weighed food records characterized dietary intake over seven consecutive days. Foods were categorized as home-prepared, away-from-home, or ready-to-eat by a registered dietitian from information provided by participants. Delay discounting was not associated with the frequency of consuming home-prepared, away-from-home, and ready-to-eat foods as reflected in the percentages of recorded foods or total energy intake from each category. However, once consuming away-from-home and ready-to-eat foods (but not home-prepared foods), impulsive women consumed more energy than less impulsive women. Exploratory analyses indicated that more impulsive women chose away-from-home foods with a higher energy density (kcal/g). Impulsivity was associated with the quantity of away-from-home and ready-to-eat foods consumed, but not the frequency of their consumption. Home food preparation may be critical to weight control for impulsive individuals.</p>

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</description>

<author>Bradley M. Appelhans et al.</author>


<category>Health Behavior</category>

<category>Obesity</category>

<category>Eating</category>

<category>Feeding Behavior</category>

<category>Impulsive Behavior</category>

<category>Fast Foods</category>

</item>






<item>
<title>Socioeconomic status, energy cost, and nutrient content of supermarket food purchases</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/251</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/251</guid>
<pubDate>Thu, 25 Oct 2012 11:13:16 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: The relative affordability of energy-dense versus nutrient-rich foods may promote socioeconomic disparities in dietary quality and obesity. Although supermarkets are the largest food source in the American diet, the associations between SES and the cost and nutrient content of freely chosen food purchases have not been described.</p>
<p>PURPOSE: To investigate relationships of SES with the energy cost ($/1000 kcal) and nutrient content of freely chosen supermarket purchases.</p>
<p>METHODS: Supermarket shoppers (n=69) were recruited at a Phoenix AZ supermarket in 2009. The energy cost and nutrient content of participants' purchases were calculated from photographs of food packaging and nutrition labels using dietary analysis software. Data were analyzed in 2010-2011.</p>
<p>RESULTS: Two SES indicators, education and household income as a percentage of the federal poverty guideline (FPG), were associated with the energy cost of purchased foods. Adjusting for covariates, the amount spent on 1000 kcal of food was $0.26 greater for every multiple of the FPG, and those with a baccalaureate or postbaccalaureate degree spent an additional $1.05 for every 1000 kcal of food compared to those with no college education. Lower energy cost was associated with higher total fat and less protein, dietary fiber, and vegetables per 1000 kcal purchased.</p>
<p>CONCLUSIONS: Low-SES supermarket shoppers purchase calories in inexpensive forms that are higher in fat and less nutrient-rich. Elsevier Inc. All rights reserved.</p>

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</description>

<author>Bradley M. Appelhans et al.</author>


<category>Adult</category>

<category>Commerce</category>

<category>Data Collection</category>

<category>Dietary Fats</category>

<category>Educational Status</category>

<category>Energy Intake</category>

<category>Female</category>

<category>Food</category>

<category>Food Analysis</category>

<category>Food Labeling</category>

<category>Food Packaging</category>

<category>*Food Preferences</category>

<category>Humans</category>

<category>Male</category>

<category>Middle Aged</category>

<category>*Nutritive Value</category>

<category>Poverty</category>

<category>Socioeconomic Factors</category>

<category>Software</category>

<category>United States</category>

</item>






<item>
<title>Correlations of clinical and laboratory measures of balance in older men and women: The MOBILIZE boston study</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/249</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/249</guid>
<pubDate>Thu, 25 Oct 2012 11:13:15 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVE: Impaired balance is associated with falls in older adults. However, there is no accepted gold standard on how balance should be measured. Few studies have examined measures of postural sway and clinical balance concurrently in large samples of community-dwelling older adults. We examined the associations among four types of measures of laboratory- and clinic-based balance in a large population-based cohort of older adults.</p>
<p>METHODS: We evaluated balance measures in the MOBILIZE Boston Study (276 men, 489 women, 64-97 years). Measures included: (1) laboratory-based anteroposterior (AP) path length and average sway speed, mediolateral (ML) average sway and root-mean-square, and area of ellipse postural sway; (2) Short Physical Performance Battery (SPPB); (3) Berg Balance Scale; and (4) one-leg stand. Spearman Rank Correlation Coefficients (r) were assessed among the balance measures.</p>
<p>RESULTS: Area of ellipse sway was highly correlated with the ML sway measures (r >0.9, p < 0.0001), and sway speed was highly correlated with AP sway (r=0.97, p < 0.0001). The Berg Balance Scale was highly correlated with SPPB (r=0.7, p<0.001), and one-leg stand (r=0.8, p<0.001). Correlations between the laboratory- and clinic-based balance measures were low but statistically significant (0.2 < r < 0.3, p<0.0001).</p>
<p>CONCLUSION: Clinic-based balance measures, and laboratory-based measures comparing area of ellipse with ML sways or sway speed with AP sway, are highly correlated. Clinic- with laboratory-based measures are less correlated. As both laboratory- and clinic-based measures inform balance in older adults but are not highly correlated with each other, future work should investigate the differences. (c) 2012 by the American College of Rheumatology.</p>

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</description>

<author>Uyen-Sa D. T. Nguyen et al.</author>


<category>Postural Balance</category>

</item>






<item>
<title>ADCC Develops Over Time during Persistent Infection with Live-Attenuated SIV and Is Associated with Complete Protection against SIV(mac)251 Challenge</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/247</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/247</guid>
<pubDate>Thu, 25 Oct 2012 11:13:13 PDT</pubDate>
<description>
	<![CDATA[
	<p>Live-attenuated strains of simian immunodeficiency virus (SIV) routinely confer apparent sterilizing immunity against pathogenic SIV challenge in rhesus macaques. Understanding the mechanisms of protection by live-attenuated SIV may provide important insights into the immune responses needed for protection against HIV-1. Here we investigated the development of antibodies that are functional against neutralization-resistant SIV challenge strains, and tested the hypothesis that these antibodies are associated with protection. In the absence of detectable neutralizing antibodies, Env-specific antibody-dependent cell-mediated cytotoxicity (ADCC) emerged by three weeks after inoculation with SIVDeltanef, increased progressively over time, and was proportional to SIVDeltanef replication. Persistent infection with SIVDeltanef elicited significantly higher ADCC titers than immunization with a non-persistent SIV strain that is limited to a single cycle of infection. ADCC titers were higher against viruses matched to the vaccine strain in Env, but were measurable against viruses expressing heterologous Env proteins. In two separate experiments, which took advantage of either the strain-specificity or the time-dependent maturation of immunity to overcome complete protection against SIV(mac)251 challenge, measures of ADCC activity were higher among the SIVDeltanef-inoculated macaques that remained uninfected than among those that became infected. These observations show that features of the antibody response elicited by SIVDeltanef are consistent with hallmarks of protection by live-attenuated SIV, and reveal an association between Env-specific antibodies that direct ADCC and apparent sterilizing protection by SIVDeltanef.</p>

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</description>

<author>Michael D. Alpert et al.</author>


<category>Antibody-Dependent Cell Cytotoxicity</category>

<category>Simian immunodeficiency virus</category>

</item>






<item>
<title>The use of cancer treatment summaries and care plans among Massachusetts physicians</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/246</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/246</guid>
<pubDate>Thu, 25 Oct 2012 11:13:12 PDT</pubDate>
<description>
	<![CDATA[
	<p>PURPOSE: Cancer survivorship presents many challenges for affected individuals and their health care providers. Reports from The Institute of Medicine document these challenges and recommend the use of survivorship treatment summaries and care plans to improve communication and coordination of care for cancer survivors. The purpose of our study was to assess current use of treatment summaries and care plans in Massachusetts and identify obstacles to greater use.</p>
<p>METHODS: A survey was mailed to cancer specialist physicians (CSPs) and primary care physicians (PCPs) in Massachusetts. The survey asked CSPs about their preparation of treatment summaries and care plans for their cancer survivor patients and perceived barriers to the provision of these documents. PCPs were asked about receipt and utility of treatment summaries and care plans and information they would like to see in these reports.</p>
<p>RESULTS: One hundred eight CSPs and 400 PCPs answered the survey. Fifty-six percent of CSPs reported that they, or their staff, prepared treatment summaries for their cancer survivor patients; however, only 14% reported preparing care plans. Fifty-four percent of PCPs reported ever receiving a treatment summary, but only 16% ever received a care plan. CSPs cited lack of training, reimbursement, and templates as barriers to preparing care plans.</p>
<p>CONCLUSIONS: Interventions are needed to make treatment summaries and care plans a part of standard care for all cancer survivors. Increasing the use of treatment summaries and care plans will require specific training and reimbursement and may be facilitated by templates that capture automated data.</p>

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</description>

<author>Anna Merport et al.</author>


<category>Neoplasms</category>

<category>Patient Care Planning</category>

<category>Physician&apos;s Practice Patterns</category>

</item>






<item>
<title>Footwear and Falls in the Home Among Older Individuals in the MOBILIZE Boston Study</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/245</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/245</guid>
<pubDate>Thu, 25 Oct 2012 11:13:11 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Whether certain types of footwear, such as slippers, socks without shoes, and going barefoot, increase the risk for falls among the elderly is uncertain. Our purpose was to examine the relationship between footwear and falls within the home in MOBILIZE Boston, a prospective cohort study of falls etiology among non-institutionalized women and men, mainly aged 70 years and older, from the Boston MA, USA area.</p>
<p>METHODS: The 765 participants were from households randomly selected from town lists. They were followed for a median of 27.5 months. At baseline, participants were administered a questionnaire that included questions on footwear usually worn, and were given a comprehensive examination that included measurement of many risk factors for falls. During follow-up participants were asked to record each day whether they had fallen; those reporting falls were asked about their footwear when they fell.</p>
<p>RESULTS: At the time of in-home falls, 51.9% of people were barefoot, wearing socks without shoes, or wearing slippers; 10.1% of people reported that their usual footwear was one of these types. Among those who fell in their own home, the adjusted odds ratio for a serious injury among those who were shoeless or wearing slippers compared to those who were wearing other shoes at the time of the fall was 2.27 (95% confidence interval 1.21-4.24).</p>
<p>CONCLUSIONS: It may be advisable for older individuals to wear shoes in their home whenever possible to minimize the risk of falling. Further research is needed to identify optimal footwear for falls prevention.</p>

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</description>

<author>Jennifer L. Kelsey et al.</author>


<category>Accidental Falls</category>

<category>Shoes</category>

</item>






<item>
<title>Reevaluating the implications of recurrent falls in older adults: location changes the inference</title>
<link>http://escholarship.umassmed.edu/prevbeh_pp/244</link>
<guid isPermaLink="true">http://escholarship.umassmed.edu/prevbeh_pp/244</guid>
<pubDate>Thu, 25 Oct 2012 11:13:10 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVES: To compare characteristics of indoor and outdoor recurrent fallers and explore some implications for clinical practice, in which a fall risk assessment for all recurrent fallers has been recommended.</p>
<p>DESIGN: Prospective cohort study.</p>
<p>SETTING: Maintenance of Balance, Independent Living, Intellect, and Zest in the Elderly of Boston Study, a study of falls etiology in community-dwelling older individuals from randomly sampled households in the Boston, Massachusetts, area.</p>
<p>PARTICIPANTS: Seven hundred thirteen women and men, mostly aged 70 and older, with at least 1 year of follow-up.</p>
<p>MEASUREMENTS: Data at baseline and from an 18-month follow-up examination were collected by questionnaire and comprehensive clinic examination. During follow-up, participants recorded falls on daily calendars. A telephone interview queried location and circumstances of each fall.</p>
<p>RESULTS: One hundred forty-five participants reported recurrent falls (>/=2) during the first year. Those who had fallen only outdoors had good health characteristics, whereas those who had fallen only indoors were generally in poor health. For instance, 25.5% of indoor-only recurrent fallers had gait speeds of slower than 0.6 m/s, compared with 2.9% of outdoor-only recurrent fallers; the respective percentages were 44.7% and 8.8% for Berg balance score less than 48. Recurrent indoor fallers generally had poor health characteristics regardless of their activity at the time of their falls, whereas recurrent outdoor fallers who fell during vigorous activity or walking were especially healthy. A report of any recurrent falls in the first year did not predict number of positive findings on a comprehensive or abbreviated fall risk assessment at the 18-month follow-up examination.</p>
<p>CONCLUSION: Characteristics of community-dwelling older people with recurrent indoor and outdoor falls are different. If confirmed, these results suggest that different types of fall risk assessment are needed for specific categories of recurrent fallers. Geriatrics Society.</p>

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</description>

<author>Jennifer L. Kelsey et al.</author>


<category>Accidental Falls</category>

<category>Activities of Daily Living</category>

<category>Aged</category>

<category>Aged, 80 and over</category>

<category>Comorbidity</category>

<category>*Environment</category>

<category>Female</category>

<category>Follow-Up Studies</category>

<category>Health Status Indicators</category>

<category>Humans</category>

<category>Interviews as Topic</category>

<category>Male</category>

<category>Prospective Studies</category>

<category>Questionnaires</category>

<category>Recurrence</category>

<category>Risk Factors</category>

</item>





</channel>
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