Brief Motivational Intervention for Physical Activity in Cancer Survivors

This study is testing a "Brief Motivational Intervention" to help cancer survivors who are part of the World Trade Center Health Program become more physically active. This intervention uses motivational interviewing, mobile health tracking, and action planning to encourage physical activity. The main goal is to see if this intervention increases your moderate to vigorous physical activity over six months. You might be able to join if you are a cancer survivor who has completed treatment, can walk slowly, and are part of the World Trade Center Health Program. People currently receiving active cancer treatment (except hormonal therapy) or with late-stage cancer cannot participate. The study is currently recruiting 84 participants.

Study design
This is an interventional study with 84 planned participants. The study does not specify a phase.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your moderate to vigorous physical activity will be measured at the beginning of the study and again at the end of the study (6 months).

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NCT07215091

Testing a Brief Motivational Intervention to Increase Physical Activity for Cancer Survivors

Recruiting
NAAll AgesInterventionalTreatment
Stony Brook University
~84 participants
Updated 2025-10-14 on ClinicalTrials.gov
What's tested:Brief Motivational Intervention

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in Moderate to Vigorous Physical Activity
Measured over Baseline to end of study (6 months)
Cancer
1 sites across 1 states
New York1

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Eligibility criteria

Inclusion

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

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.
  • Change in Moderate to Vigorous Physical ActivityBaseline to end of study (6 months)

    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.