A Dyadic Intervention for Young Adult Patients with Cancer and Their Partner Caregivers
- Conditions
- Psychological DistressCancerCaregiver BurdenCouplesSurvivorshipCoping Skills
- Interventions
- Behavioral: Young Adults Coping with Cancer Together Intervention
- Registration Number
- NCT06172907
- Lead Sponsor
- Massachusetts General Hospital
- Brief Summary
The purpose of this pilot study is to examine the feasibility and acceptability of a brief psychotherapy intervention to improve psychosocial coping and maintain couple relationships among young adults (aged 25-39) with cancer and their caregiving partners.
- Detailed Description
Young adults (YA) with cancer have unique challenges in coping, and their primary partners may experience burden and low self-efficacy related to caregiving. In this single-arm pilot trial, the investigators shall deliver an eight-session intervention to YAs with cancer and their self-identified partners who provide caregiving. The intervention is founded on principles from cognitive-behavioral therapy and couples-focused interventions, tailored for YA. The aim of the study is to assess the feasibility and acceptability of the intervention, which will inform refinements prior to a larger-scale clinical trial. This study will include 10 YAs and their partner-caregivers (N=20). Participants will complete surveys at baseline and after the intervention, and will be invited to complete optional semi-structured exit interviews.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 20
- Either: (1) Currently receiving active cancer treatment (n=5) or are within two years of completing active treatment (n=5) at Massachusetts General Cancer Center (MGHCC), located in Boston, Massachusetts, United States, OR (2) are the partner of an individual between the ages of 25-39 who is currently receiving treatment at MGHCC (n=5) or who has completed cancer treatment at MGHCC within the past two years (n=5)
- Either: (1) Indicates a score ≥4 on the National Comprehensive Cancer Network (NCCN) adapted distress thermometer study screening questions, OR (2) are the partner of a participant indicating a score ≥4 on the NCCN adapted distress thermometer study screening questions
- English-speaking
• Uncontrolled psychosis, active suicidal ideation, or cognitive impairment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Young Adults Coping with Cancer Together Intervention Young Adults Coping with Cancer Together Intervention Young adults with cancer and their partner-caregivers will attend dyadic virtual psychotherapy sessions lasting 45-60 minutes on a weekly basis for eight weeks.
- Primary Outcome Measures
Name Time Method Feasibility of Intervention 10 +/- 2 Weeks Feasibility will be measured by measured by participant rates of enrollment (≥50% of those eligible), participant retention (≥70% of those enrolled), and intervention attendance (≥70% attending at least 6 of 8 sessions).
Acceptability of Intervention 10 +/- 2 Weeks Acceptability with be measured by satisfaction with the intervention as rated on the Client Satisfaction Questionnaire. The intervention will be deemed acceptable if ≥75% of participants report average satisfaction that exceeds the CSQ's midpoint.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (4)
Massachusetts General Hospital Cancer Center
🇺🇸Boston, Massachusetts, United States
Emerson Hospital/MGH Cancer Center
🇺🇸Concord, Massachusetts, United States
Mass General at North Shore Cancer Center
🇺🇸Danvers, Massachusetts, United States
Mass General at Newton Wellesley Hospital
🇺🇸Newton, Massachusetts, United States