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Effectiveness and Implementation of a Brief Motivational Intervention to Increase Physical Activity for World Trade Center Health Program Cancer Survivors

NCT ID: NCT07215091Sponsor: Stony Brook UniversityLast updated: 2025-10-14

Summary

The goal of this study is to test a brief motivational intervention to increase physical activity in a group of cancer survivors who are participants in the World Trade Center Health Program.

Detailed description

The World Trade Center Health Program (WTCHP) tracks the ongoing health and well-being of over 91,000 first responders and people who lived and worked near the World Trade Center. Research has established that WTCHP members are at higher risk for a constellation of health conditions, including cancer. Cancer survivors, the focus of this study, are at risk for physical and functional impairment. As WTCHP members with cancer age, developing pragmatic interventions to mitigate physical decline is an important next step in a coordinated program of care and research in this vulnerable population. Physical activity (PA) interventions are strong candidates for investigation, given that physical inactivity in WTCHP members has been correlated with respiratory illness, poor sleep, and PTSD. PA has many health benefits, yet interventions to support PA are not routinely incorporated into clinical practice. Evidence-based guidelines recommend PA counseling in clinical care and health professionals believe they should be doing this. However, a gap remains in implementing PA interventions at the point of care. This study will test an evidence-based motivational intervention to initiate and maintain PA among WTCHP particpatants with cancer.

Arms & interventions

  • BehavioralBrief Motivational Intervention

    The study includes a 3-component motivational intervention based on the Theory of Planned Behavior. The components include motivational interviewing (MI); mobile health monitoring; and action planning. MI is used to build a positive attitude towards physical activity (PA). Mobile health monitoring will be conducted with a Fitbit to monitor steps per day. The last component of the intervention includes action planning to design a PA program that fits their abilities and lifestyle. The research team will develop a PA grid that includes aerobic, strength, and flexibility PA options. The PA grid provides an opportunity to personalize the action plan by choosing from a 'menu' to match interests. Following the in-person baseline visit, participants will be called approximately every 2 weeks (4-5 phone contacts) during the 3-month intervention period to review and update their action plan.

Outcome measures

Primary

  • Change in Moderate to Vigorous Physical Activity

    The primary outcomes will be measured with Fitbit data. Fitbit software allows classification of each minute as being in sedentary, light, moderate, or vigorous activity, and provides metabolic equivalents (METs) for each minute. Positive changes in levels of physical activity will be determined by a 25% increase in MVPA from baseline to end of intervention. This estimation is based on a systematic review of motivational physical activity interventions in cancer survivors (Takemura, 2024). This change in outcome measure is well justified and sensitive to small changes in activity.

    Time frame: Baseline to end of study (6 months)

Secondary

  • Quality of Life (SF-20)

    Time frame: Baseline to end of study (6 months)

  • Sleep (PROMIS Sleep SF)

    Time frame: Baseline to end of study (6 months)

  • Fatigue (PROMIS Fatigue SF)

    Time frame: Baseline to end of study (6 months)

  • Physical Functioning (Short Physical Performance Battery)

    Time frame: Baseline to end of study (6 months)

  • Post traumatic stress disorder (PCL-5)

    Time frame: Baseline to end of study (6 months)

Eligibility criteria

Sex: AllAge: All agesHealthy volunteers: No
Inclusion Criteria: * Participation in the World Trade Center Health Program * History of cancer, completed treatment * Ability to be physically active (at minimum be able to walk slowly) Exclusion Criteria: * Participants receiving active cancer treatment (excluding hormonal therapy); * Late-stage cancer (metastatic); * Inability to follow the scheduled visits; * Women who are pregnant * Patients who would not be safe exercising without medical supervision (ECOG score of 3, significant comorbidities, unable to even walk slowly) * Inability to speak and read English.

Study locations (1)

Stony Brook University

Stony Brook, New York, 11794-8240

Recruiting
Pamela Ginex, EdD, MPH, RN · Contact
Pamela K Ginex, EdD, MPH, RN · Principal Investigator
Testing a Brief Motivational Intervention to Increase Physical Activity for Cancer Survivors | Cancerify