The purpose of this study is to develop and pilot test a behavioral intervention for elderly adults in treatment for colon cancer, to enhance their skills for managing the challenges of completing chemotherapy regimens. The investigators will assess feasibility and acceptability of the intervention, and explore preliminary efficacy of the intervention for reducing psychological distress and improving rates of optimal chemotherapy adherence.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
15
Two or three one-hour sessions of an individual behavioral intervention led by a doctoral-level licensed psychologist during the first 12 weeks of chemotherapy. Intervention addresses modifiable behaviors for managing chemotherapy challenges.
Massachusetts General Hospital
Boston, Massachusetts, United States
Participant satisfaction with intervention structure, timing and content
Participants rate acceptability of structure, timing and content of intervention using Likert-type response scales, and are also invited to provide brief qualitative feedback on opinions about intervention.
Time frame: At approximately 12 weeks post-baseline
Number of participants who withdraw from study after enrollment
Time frame: At approximately 12 weeks post-baseline
Change from baseline in the Hospital Anxiety and Depression Scale
Time frame: At approximately 12 weeks post-baseline
Change from baseline in the Symptom Distress Scale
The 13-item Symptom Distress Scale (SDS)measures physical and psychological symptom-related distress.
Time frame: At approximately 12 weeks post-baseline
Proportion of each chemotherapy component administered during the treatment regimen relative to the total planned amount
Time frame: At approximately 24 weeks post-baseline
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.