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ACTIVE NOT RECRUITING
NCT00498875

Depression and Adherence in Head and Neck Cancer

Sponsor: M.D. Anderson Cancer Center

View on ClinicalTrials.gov

Summary

Primary Objectives: * Develop and pilot test an innovative intervention to determine its feasibility and acceptability to patients. Recruitment rate, patient satisfaction, attendance, questionnaire completion rates and the reliability and validity of the questionnaires will be assessed. * Conduct preliminary analyses on the efficacy of the intervention in improving patients' depression. Evaluate whether depression levels in patients receiving the intervention decreases, and whether the decrease is greater among those who complete more sessions. * Test the relationship between patients' depression levels and adherence to swallowing rehabilitation and to dental preventive maintenance regimens.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

185

Start Date

2005-03-15

Completion Date

2026-12-31

Last Updated

2026-03-09

Healthy Volunteers

No

Interventions

BEHAVIORAL

Questionnaire

Questionnaire regarding mood, coping with cancer, how closely you follow your treatment schedule, your thoughts, your demographic information (such as age and race), and your medical history. If the answers to your questionnaire indicate that you may be depressed, you will be offered the intervention portion of the study.

BEHAVIORAL

Depression Intervention

Sessions given over 7 weeks and each lasting 30-45 minutes, that use "cognitive-behavioral" techniques.

Locations (1)

University of Texas MD Anderson Cancer Center

Houston, Texas, United States