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Feasibility of a Novel, Theory Based Physical Activity Intervention Among Adult Cancer Survivors

Designing and Testing the Feasibility of a Theory-Based Intervention to Promote Physical Activity Among Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04498130
Enrollment
29
Registered
2020-08-04
Start date
2021-10-02
Completion date
2022-12-31
Last updated
2023-01-31

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

Conditions

Cancer Survivors, Exercise, Sedentary Behavior

Brief summary

As the number of cancer survivors grows and expected survival time increases, the health behaviors of this population are gaining significant attention from the research and public health community. Adoption or maintenance of healthy lifestyles after cancer has the potential to reduce both cancer- and non-cancer-related morbidity and mortality. Exercise adoption and maintenance remains a significant challenge for adults, especially clinical populations such as cancer survivors who may struggle with comorbidities, symptoms and side-effects of the disease or medications, and overall compromised health and functioning. A number of site-based exercise interventions have been conducted to promote physical activity, often using a theoretical basis to design and execute the intervention. Although these programs are successful in exposing cancer survivors to regular physical activity, they often struggle with exercise maintenance after the conclusion of the structured site-based group exercise sessions. The goal of the proposed project is to enhance physical activity engagement among adult cancer survivors by designing a home-based program using the socio-ecological framework and employing constructs from social cognitive theory to guide participants through the project.

Interventions

BEHAVIORAL12-Week Home Exercise Group

12 week home-based program consisting of: weekly Zoom group chats; exercise videos; free exercise equipment and pedometer; an exercise manual with worksheets to promote increased physical activity; access to a unique group social media page

BEHAVIORALEducation Comparison Group

12 week home-based program consisting of: weekly check-in phone calls; exercise videos; free exercise equipment and pedometer; an exercise manual with worksheets to promote increased physical activity; access to a unique group social media page.

Sponsors

University of Illinois at Urbana-Champaign
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* 30-75 years of age at baseline * Cancer diagnosis during adulthood (no childhood cancers) * Low-active (≤ 2 days of 30 minutes of structured exercise/week) * At least 1 month since last cancer treatment (surgery, chemotherapy and/or radiation) * No reservations from a doctor/physician/oncologist to engage in physical activity * Not currently undergoing cancer-related treatment * No active cancer diagnosis * Willingness to participate in a 12-week home exercise program * Willingness to be randomized to either the 12-week home exercise or a 12 week education group * Access to a laptop/ phone with Zoom web-conferencing software * An active email address to receive and sign the electronic informed consent * Willingness to complete study questionnaires before and after the 12-week program, and 3 months after the program * Fluency in English

Exclusion criteria

* Below 30 or above 75 of age at baseline * Childhood cancer diagnosis only * High active (\> 2 days of 30 minutes of structured exercise/week) * Cancer treatment within the last month or currently undergoing treatment * Advised to refrain from physical activity by a doctor/physician/oncologist * Active cancer diagnosis * Not willing to participate in a 12-week home exercise group and/or complete study assessments * Not willing to be randomized into one of the two study groups * No access to a laptop/phone with Zoom software * No access to active email * Not fluent in English

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of Zoom-Based Exercise Coaching12 weeksParticipants in the intervention arm will answer Likert-format questions relating to their preference, tolerance and usage of the Zoom-based group meetings to promote physical activity levels. The scale will use a 1-5 rating, with 1 being lowest preference/displeased and 10 being the highest preference/very pleased.
Change in average daily step countBaseline, 12 weeks, 24 weeksParticipants will wear a hip-based pedometer for 7 days at baseline, 12 weeks and 24 weeks.
Change in minutes of daily sedentary timeBaseline, 12 weeks, 24 weeksThe Sedentary Behavior Questionnaire (developed by Rosenberg et al., 2010) will be administered at baseline,12 weeks and 24 weeks to assess participants' time spent sitting. Questions relating to sedentary behavior cover both weekday and weekend sitting time, as well as domain-specific sedentary behaviors (i.e. occupational, transportation, and leisure sitting time).Response options for the amount of time engaged in each behavior include: none, 15 minutes or less, 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, or 6 hours or more. For scoring, the time spent in each behavior is converted into hours, and the hours per day for each item are summed separately for weekdays and weekend days. Higher scores indicate higher amounts of daily sitting time.

Secondary

MeasureTime frameDescription
Use of the exercise manual12 weeksParticipants in both groups will answer Likert-format questions relating to their preference, usage and perceived helpfulness of the study-specific exercise manual. The scale will use a 1-10 rating, with 1 being lowest preference/displeased and 10 being the highest preference/very pleased.
Change in physical activity engagementBaseline,12 weeks, 24 weeksThe Godin-Shepard Leisure Time Exercise Questionnaire will be administered at baseline, 12 weeks and 24 weeks to assess individuals' reported weekly frequency of engaging in light, moderate and strenuous vigorous-intensity exercise. For each intensity level, participants will report the number of times per week they engaged in an exercise bout \>=10 minutes and the average duration of the bouts. For each intensity level, the number of bouts per week will be multiplied by the average duration per bout to reflect participant's average activity level.

Countries

United States

Outcome results

None listed

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