Protocol for a randomized controlled trial of brief behavioral activation among older adult cancer survivors.
Rebecca M Saracino, Ellen Y Park, Caraline Demirjian...
https://pubmed.ncbi.nlm.nih.gov/38342735/Actively Recruiting
Led by Memorial Sloan Kettering Cancer Center · Updated on 2026-06-22
90
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying whether a psychotherapy method called behavioral activation BA can be effectively delivered remotely by phone or video to treat depression in older adult cancer survivors. This study compares BA with supportive psychotherapy, aiming to understand if these approaches can improve depressive symptoms in this population. The trial is a phase 2, randomized, double-blind study sponsored by Memorial Sloan Kettering Cancer Center. Participants will receive either behavioral activation or supportive psychotherapy, both provided remotely via video-conference or telephone based on patient preference. Full participants will have ten weekly sessions lasting 30 to 50 minutes over about 10 weeks. Training case participants will receive the same number of sessions over approximately 5 weeks. These interventions are designed to be accessible and flexible for older adults. Throughout the study, participants will be evaluated using the Patient Health Questionnaire 9 PHQ-9 to measure depression levels, with the primary outcome assessed two months after the intervention ends. Eligibility includes being 65 or older, having a history of cancer, and meeting cognitive and communication abilities for remote sessions. Safety is monitored by excluding those requiring higher levels of care for suicidal ideation or with significant psychiatric disorders. The study lasts up to the primary completion date in June 2027.
CONDITIONS
A Study of Brief Behavioral Activation for the Treatment of Depression in Older Adult Cancer Survivors
R
Rebecca Saracino, PhD
C
Christian Nelson, PhD
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Memorial Sloan Kettering Cancer Center
Lead Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | Brief Behavioral Activation | Supportive Psychotherapy |
|---|---|---|
| What is it? | A structured, short-term behavioral treatment that aims to reduce depression by helping participants engage in valued activities and address avoidance patterns. | A talk therapy focused on providing emotional support and helping participants discuss their feelings and cope with challenges related to depression and survivorship. |
| Role in the study | Examined as the main intervention being tested for reducing depressive symptoms in older adult cancer survivors. | Serves as the comparator intervention for evaluating whether Brief Behavioral Activation yields different or greater benefit. |
| Primary use | Designed to treat depression by increasing positive and meaningful activities and decreasing unhelpful avoidance behaviors. | Aims to support emotional well-being through supportive conversation and coping strategies rather than structured behavioral change. |
| How is it given? | Delivered remotely by video conference or phone in 10 weekly sessions, each lasting 30 to 50 minutes, guided by a structured protocol. | Delivered remotely by video conference or phone in 10 weekly sessions, each lasting 30 to 50 minutes, following a flexible supportive therapy framework. |
| Evidence status | Efficacy for depression in older adult cancer survivors is being studied; initial results are not yet established for this population in this trial setting. | Effectiveness for depression in older adult cancer survivors is also being actively studied, with results not yet available for this clinical setting. |
| Important limitations | Long-term depression outcomes and effects specifically for older adult cancer survivors are not yet established. Results from other populations may not fully apply. | Supportive Psychotherapy's long-term effects and direct comparative effectiveness for depression in this population remain under investigation and are not yet known. |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Approximately 10 weeks
Participants receive either behavioral activation or supportive psychotherapy remotely via video or telephone. Sessions are approximately weekly, each lasting 30 to 50 minutes, over about 10 weeks.
Ten sessions, once per week
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Rebecca M Saracino, Ellen Y Park, Caraline Demirjian...
https://pubmed.ncbi.nlm.nih.gov/38342735/Memorial Sloan Kettering Cancer Center
Lead Sponsor