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Trial Title:
Digital Connections: an EHealth Group Intervention for Young Adult Cancer Survivors
NCT ID:
NCT05952492
Condition:
Cancer
Study type:
Interventional
Study phase:
N/A
Overall status:
Active, not recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Primary purpose:
Supportive Care
Masking:
None (Open Label)
Intervention:
Intervention type:
Behavioral
Intervention name:
Stress Management Skills Training
Description:
Participants will attend group sessions with a trained facilitator held over
videoconference. Sessions will each last 2 hours and be held once weekly for 10 weeks.
Sessions will include stress management skills training and health education content.
Arm group label:
Stress Management Skills Training
Summary:
The purpose of this study is to determine the feasibility of recruiting young adult
cancer survivors from across the nation and to explore the impact of an eHealth group
intervention on psychosocial health in this population.
Detailed description:
Study investigators will conduct a single-arm pilot trial in which a 10 week eHealth
group intervention will be delivered via a study website. We will use a multi-pronged
approach to recruit young adult cancer survivors from across the country. Study
participants will attend weekly group meetings with a trained facilitator to receive the
manualized intervention over the course of 10 weeks.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
1. Aged 18-39 years at the time of participation
2. Diagnosed with any invasive cancer between 15-39 years old
3. Finished curative cancer treatment 1 month to 5 years prior to enrollment (except
maintenance therapy such as ongoing hormone therapy)
4. Currently experiencing at least mild symptoms of depression or anxiety (i.e., score
≥1 on the Patient Health Questionnaire-4)
5. Able to speak and read English so all group attendees can communicate in a shared
language.
6. Able and willing to give informed consent.
7. Access to internet or cellular connectivity with sufficient bandwidth to participate
in videoconferences
Exclusion Criteria:
1) Documented or observable psychiatric or neurological disorders that could interfere
with study participation (e.g., psychosis, active substance abuse)
Gender:
All
Minimum age:
18 Years
Maximum age:
39 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
University of Arizona Cancer Center
Address:
City:
Tucson
Zip:
85719
Country:
United States
Start date:
January 16, 2024
Completion date:
October 25, 2024
Lead sponsor:
Agency:
University of Arizona
Agency class:
Other
Source:
University of Arizona
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05952492
