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AYActive Study! A Physical Health Activity Intervention

AYActive Study! A Physical Health Activity Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04601948
Enrollment
14
Registered
2020-10-26
Start date
2019-11-06
Completion date
2020-09-04
Last updated
2023-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Adolescents, Young Adults

Brief summary

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.

Detailed 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.

Interventions

BEHAVIORALmHealth Activity Intervention

Eligible participants will receive a Fitbit activity monitor and access to our 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.

Sponsors

University of Iowa
CollaboratorOTHER
Lucas Carr
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

The intervention will include an 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.

Eligibility

Sex/Gender
ALL
Age
13 Years to 39 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Number of steps taken per dayDail steps will be measured each day of the intervention for 7 weeksNumber of steps taken per day on each day of the intervention

Secondary

MeasureTime frameDescription
PROMISE Pain ScaleChange in pain over 7 weeks8 item scale, lower score is better
PROMIS Physical Function ScaleChange in physical function over 7 weeks8 item scale, lower score is better
PROMIS Depression ScaleChange in depression over 7 weeks8 item scale, lower score is better
PROMIS Fatigue ScaleChange in fatigue over 7 weeks8 item scale, lower score is better
Exercise Self-Regulatory EfficacyChange in exercise self regulatory efficacy over 7 weeks20 item scale, higher score is better
Social Support for exerciseChange in social support for exercise over 7 weeks13 item scale, higher score is better
PROMIS Anxiety ScaleChange in anxiety over 7 weeks8 item scale, lower score is better

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026