Lifestyle Intervention for Veterans With Blood Cancer: Tele-Intervention

ConditionBlood Cancers
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVA Pittsburgh Healthcare System

About this trial

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.

Eligibility criteria

Qualifiers

Living with blood cancer

Physically willing and able to perform 30-90 minutes of exercise a minimum of 2 times per week

Disqualifiers

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

Trial design

Treatments tested in this trial

  • EXERCISE TRAINING WITH OR WITHOUT MEDICATION

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators

VA Pittsburgh Healthcare System

Lead sponsor

The Leukemia and Lymphoma Society

Collaborator