Dosing Physical Activity Among Older Cancer Survivors Who Experience Chronic Pain: a Micro-randomized Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorMedical College of Wisconsin

About this trial

The purpose of this study is to assess the best time to deliver a message to increase physical activity and how often participants will experience a pain episode in the 24 hours following their receipt of a message to increase physical activity.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age greater than or equal to 65 years.

Patients with a history of bladder, breast, cervical, colorectal, endometrial, lung, and prostate cancer diagnosis and treatment.

Fluent in spoken and written English.

Patient has access to smartphone

Disqualifiers

Patient has metastatic disease.

Patient has cancer recurrence.

Trial design

Design model

Single group

Treatments tested in this trial

  • Physical Activity Promotion Intervention

    Behavioral

    This physical activity promotion intervention is a micro-randomized trial designed to determine the most effective time to send a message to promote physical activity among cancer survivors who experience chronic pain symptoms.

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Micro-randomized trial study armExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

ActiGraph accelerometer measured physical activity behaviors (sedentary, light, moderate, vigorous intensity).

Physical activity will be measured using an ActiGraph accelerometer. Data will be aggregated into physical activity estimations (sedentary, light, moderate, vigorous, steps, etc.) using standard methods. Outcome of interest will be probability older cancer survivors are physically active in the 30 minutes following the receipt of a messaging prompt to promote physical activity.

Time frame
4 weeks
2

11-point box scale to assess pain on a scale of 0 (no pain) to 10 (worst possible pain).

Pain state will be assessed by response to the pain rating measured by the 11-Point Box Scale in the study app. Participants will receive a smart phone prompt to rate their pain 4 times per day. Outcome of interest will be probability older cancer survivors experience a pain episode in the 24 hours following the receipt of a messaging prompt to increase physical activity.

Time frame
4 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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Medical College of Wisconsin

Lead sponsor

National Cancer Institute (NCI)

Collaborator