Title

Patient compliance and medical research: issues in methodology

UMMS Affiliation

Department of Quantitative Health Sciences

Date

2-1-1994

Document Type

Article

Medical Subject Headings

*Appointments and Schedules; *Drug Therapy; Humans; *Patient Compliance; *Research Design

Disciplines

Bioinformatics | Biostatistics | Epidemiology | Health Services Research

Abstract

Compliance with medication and medical appointments is presumed to have a critical influence on outcomes of medical interventions. However, compliance may not always be easily defined or accurately measured. No single method of measuring compliance with appointments or medication is applicable in all settings. The apparent effects of compliance on outcome may be both direct and indirect; research is needed to define more clearly how these effects may be mediated. Identifying effective methods of enhancing compliance requires accurate methods of measuring compliance. In addition, the effectiveness of interventions may decay over time, and differences in effectiveness in acute versus long-term settings have not been well studied. Researchers conducting clinical trials of medical interventions must evaluate compliance in the population studied and consider the potential impact of noncompliance on trial results and their generalizability. In some trial designs, data may best be analyzed by considering compliance a dependent or an outcome variable. Under appropriate circumstances, compliance may be considered an independent variable. Readers of the medical literature should consider how compliance was measured and analyzed when interpreting the results of clinical trials. Table 4 suggests criteria for critical appraisal of compliance-related issues in reports of clinical trials.

Rights and Permissions

Citation: J Gen Intern Med. 1994 Feb;9(2):96-105.

Related Resources

Link to Article in PubMed