Lifestyle Intervention for Veterans With Blood Cancer: Tele-Intervention
Recruiting now · Not applicable
Conditions studied: Blood Cancers
In brief
Background. This study aims to evaluate the effectiveness of a telehealth-mediated lifestyle intervention program tailored for veterans with blood cancer, focusing on improving health-related quality of life, mental health, and pain outcomes. The hypothesis posits that the telehealth-delivered program will lead to significant improvements in these areas, specifically targeting veterans undergoing treatment or in post-treatment phases. Objective. Recognizing the unique experiences of veterans, especially those in rural or underserved regions, this study seeks to provide insights into the feasibility and impact of telehealth-based lifestyle interventions for this distinct population. Methods. The pilot trial will enroll 30 veterans from the H. John Heinz III VA. Participants will complete baseline web-based surveys assessing demographics, occupational performance, and telehealth preparedness. The intervention comprises progressive resistance and aerobic exercises delivered via telehealth by a health coach, starting with a live supervised session followed by regular remote sessions. Each participant will engage in exercise sessions coordinated through the Veteran's Video Connect (VVC) application, with ongoing communication facilitated via email. This setup allows the health coach to adjust exercise intensity based on real-time symptom feedback. To address potential technology literacy biases, the VVCMatch assessment will categorize veterans as "technology prepared" or in need of additional education. Those requiring support will receive guidance on using the VVC app before starting the intervention. Additionally, participants will receive dietary consultations from the Leukemia and Lymphoma Society, independent of the research team. Outcome measures include assessments of symptoms, fatigue, function, mental health, and pain, along with evaluations of the intervention's usability through surveys on perceived usefulness and ease of use. These assessments aim to detect meaningful changes and ensure the intervention's effectiveness and acceptability among veterans.
Key facts
- Study ID
- NCT07058571
- Run by
- VA Pittsburgh Healthcare System
- People needed
- 30
- Starts
- 2015-04-03
- Expected to finish
- 2026-05-31
- Last updated by the study team
- 2025-07-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Living with blood cancer
- Physically willing and able to perform 30-90 minutes of exercise a minimum of 2 times per week
You may not qualify if…
- Veterans who are unable to perform 30-90 minutes of exercise twice a week
- Veterans with significant disabilities related to balance or motion that would cause a safety risk
- Veterans without a smart personal device (smart phone, tablet, or computer) and internet connection (for example, cellular or WIFI connection)
- Veterans who are pregnant
Where it is running
- VA Pittsburgh Healthcare System — Pittsburgh, Pennsylvania, United States (enrolling)
Full record on ClinicalTrials.gov
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