AYActive Study! A Physical Health Activity Intervention

Lucas Carr

Status: Completed

Conditions: Cancer

Treatments: Behavioral: mHealth Activity Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT04601948

201907702

Details and patient eligibility

About

The purpose of this pilot study is to explore the feasibility, acceptability, and efficacy of a 6-week mobile health (mHealth) physical activity intervention among adolescent and young adult (AYA) cancer survivors being treated at the University of Iowa Hospitals and Clinics.

Full description

The purpose of this pilot study is to explore the feasibility, acceptability, and efficacy of a 6-week mobile health (mHealth) physical activity intervention among adolescent and young adult (AYA) cancer survivors being treated at the University of Iowa Hospitals and Clinics. Eligible participants will receive a Fitbit activity monitor and access to the mHealth physical activity intervention for 6 weeks. The intervention will include regular motivational messages to encourage activity, a social media thread to provide social support, and a series of fun virtual walking races. AYA cancer survivors between 13-39 years are invited to participate and the impact of this intervention will be tested over 6 weeks.

Enrollment: 14 patients

Sex: All

Ages: 13 to 39 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Male and female cancer survivors
• Diagnosed between 13 and 39 years old
• Currently 3-24 months post-treatment (or in maintenance therapy)
• Receiving survivorship care at HCCC/UIHC
• In remission
• Physically able to walk without limitations
• Own a smartphone with a data plan that is also capable of receiving and sending texts
• Able to understand English and provide informed assent/consent

Exclusion criteria

• Physically unable to walk without limitations
• Actively receiving cancer treatment
• Does not own a smartphone with a data plan
• Visual or cognitive impairments causing inability to read, complete or sign the consent form and survey
• Participants with diagnosis of thyroid cancer (due to differences in physical, psychological, emotional, and social effects)
• Presence of a psychiatric disorder that is not managed/unstable or suicidal ideation/actuation in preceding 12 months
• Currently meeting physical activity requirements per American Cancer Society guidelines (150 or more minutes per week of moderate to vigorous physical activity)

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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14 participants in 1 patient group

Intervention

Experimental group

Description:

Participants will receive a Fitbit activity monitor and access to the mHealth physical activity intervention for 6 weeks. The intervention will include regular motivational messages to encourage activity, a social media thread to provide social support, and a series of fun virtual walking races.

Treatment:

Behavioral: mHealth Activity Intervention