Developing and Pre-Testing an eHealth Group Intervention for Young Adult Cancer Survivors
- Conditions
- Cancer
- Interventions
- Behavioral: Cognitive-Behavioral Stress Management and Health Education
- Registration Number
- NCT05054569
- Lead Sponsor
- Northwestern University
- Brief Summary
The purpose of this study is to develop and pre-test an eHealth group intervention for young adult cancer survivors.
- Detailed Description
In the first part of this study, the investigators adapted an evidence-based intervention for improving HRQOL to better meet the needs of young adult cancer survivors, and then conducted focus groups with young adult cancer survivors to get feedback on the adapted intervention. In the second part of the study, the investigators will conduct a single-arm pilot trial in which the adapted intervention will be delivered over videoconference via weekly group meetings with a trained facilitator over the course of 10 weeks.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 6
- age 18-39 years at the time of participation
- diagnosed with a non-metastatic primary cancer between 18-39 years old
- completed primary cancer treatment (excepting hormone therapy) 1 month to 5 years prior to enrollment
- able to speak and read English
- access to internet or cellular connectivity with sufficient bandwidth to participate in videoconferences
- metastatic disease
- psychiatric or neurological disorders that could interfere with study participation
- considered part of a vulnerable population
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description 10-week eHealth intervention Cognitive-Behavioral Stress Management and Health Education Weekly video conference groups led by a trained facilitator
- Primary Outcome Measures
Name Time Method Acceptability of the adapted intervention Immediately after the intervention Immediately after the intervention participants will report their satisfaction with the full program through a brief survey.
- Secondary Outcome Measures
Name Time Method Change in coping from baseline to immediately after the intervention Baseline and immediately after the intervention Participants will complete the Brief Coping Orientation to Problems Experienced scale, which yields 14 two-item subscales. Subscale scores range from 2 to 8, with higher scores indicating greater usage of the coping strategy being assessed.
Change in cancer-related distress from baseline to immediately after the intervention Baseline and immediately after the intervention Participants will complete the 22-item Impact of Event Scale-Revised. Scores range from 0 to 88, with higher scores indicating greater cancer-related distress.
Change in stress management skills self-efficacy from baseline to immediately after the intervention Baseline and immediately after the intervention Participants will complete subscales from the Measure of Current Status. Subscale scores range from 0 to 8, 0 to 12, or 0 to 20 depending on the subscale. Higher scores indicate more of the construct being assessed.
Change in symptom burden from baseline to immediately after the intervention Baseline and immediately after the intervention Participants will complete a modified version of the Edmonton Symptom Assessment Scale, which assesses 10 common cancer-related symptoms each on a numerical rating scale ranging from 0 to 10. Higher scores indicate greater symptom burden.
Change in health-related quality of life (HRQOL) from baseline to immediately after the intervention Baseline and immediately after the intervention Participants will complete the 27-item Functional Assessment of Cancer Therapy - General. Scores range from 0 to 108, with higher scores reflecting better quality of life.
Trial Locations
- Locations (1)
Northwestern University Feinberg School of Medicine
🇺🇸Chicago, Illinois, United States