Caregivers-Patients Support Coping With Advanced-Cancer (CASA) Intervention
Enrolling by invitation · Not applicable · Has a placebo group
Conditions studied: Advanced Cancer, Caregivers, Patients, Stage III Cancer, Stage IV Cancer
In brief
This pilot aims to prepare the PI to receive hands-on experience in implementation and dissemination and design and lead pilot studies in palliative care. The catchment area communities experience lower cancer health outcomes and are more likely to be diagnosed with advanced cancer when compared to other surrounding areas. The PI's catchment area experiences advanced cancer, and their caregivers are at an increased risk for unmet psychosocial needs; this pre-pilot will allow the PI to focus on this critical gap in equal healthcare. The research goal of this proposal is to refine and pre-pilot an intervention titled Caregivers Patients Support to Cope with Advanced Cancer (CASA), a five-session, 60-minute telehealth series for patient-caregiver dyads. The rationale for this project is that it will lay the groundwork for a Randomized Control Trial (RCT) testing the efficacy of CASA. It will also assess the implementation of an innovative method to deliver the CASA intervention. This study aims to use the collaborative intervention planning framework and ORBIT model to modify and assess the feasibility and preliminary effect of the CASA intervention. The overall impact of this study is to improve access to psychosocial interventions in the proposed catchment area.
Key facts
- Study ID
- NCT06883058
- Run by
- Ponce Medical School Foundation, Inc.
- People needed
- 62
- Starts
- 2026-01-01
- Expected to finish
- 2027-07-30
- Last updated by the study team
- 2026-06-09
Who can join
Age: 21 and older, up to 105. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Cancer patients must be stage III and IV solid tumor patients who report distress >4 on the Distress Thermometer
- Caregivers. Identified caregivers by distressed patients.
You may not qualify if…
- diagnosed with a major disabling medical or psychiatric condition
- unable to understand the consent procedure, or (3) too ill to participate, all as reported by the participant and/or determined by the investigator's judgment.
Where it is running
- Ponce Research Institute — Ponce, PR, Puerto Rico
Full record on ClinicalTrials.gov
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