Depression and Adherence in Head and Neck Cancer
Running, not enrolling
Conditions studied: Oropharyngeal Cancer, Head and Neck Cancer
In brief
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 facts
- Study ID
- NCT00498875
- Run by
- M.D. Anderson Cancer Center
- People needed
- 185
- Starts
- 2005-03-15
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2026-03-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Stage I-IV
- At least 18 years of age
- Speak and read English at a 7th grade level
- Are oriented to time, person, and place
- Have a Zubrod performance status of 0-3.
- To be eligible for the pilot depression intervention patients must score 9 or above on the Patient Health Questionnaire (PHQ-9). Additionally, if a patient has an elevated PHQ score and does not meet the cutoff but expresses a desire to be in the intervention in order to relieve his or her depression, then the PI will contact the participant to further assess eligibility for the intervention. Patients who do not make the cut-off will still be included in the study's statistical analyses.
You may not qualify if…
- Do not have other cancer diagnoses, excepting non-melanoma skin cancer.
Where it is running
- University of Texas MD Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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