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
1 other identifier
interventional
29
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 23, 2020
CompletedFirst Posted
Study publicly available on registry
August 4, 2020
CompletedStudy Start
First participant enrolled
October 2, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2022
CompletedJanuary 31, 2023
January 1, 2023
1.2 years
March 23, 2020
January 27, 2023
Conditions
Outcome Measures
Primary Outcomes (3)
Feasibility of Zoom-Based Exercise Coaching
Participants 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.
12 weeks
Change in average daily step count
Participants will wear a hip-based pedometer for 7 days at baseline, 12 weeks and 24 weeks.
Baseline, 12 weeks, 24 weeks
Change in minutes of daily sedentary time
The 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.
Baseline, 12 weeks, 24 weeks
Secondary Outcomes (2)
Use of the exercise manual
12 weeks
Change in physical activity engagement
Baseline,12 weeks, 24 weeks
Study Arms (2)
12-Week Home Exercise Group
EXPERIMENTALThe 12-week theory-based physical activity intervention will involve mailing participants an exercise manual with health and exercise information (i.e. information about exercising safely, modules related to the social cognitive theory, weekly goal setting worksheets, exercise-tracking logs, etc.), a resistance band, and a standard Omron pedometer. Participants will receive a weekly 30-minute Zoom--based group meetings to discuss different strategies to begin and maintain a consistent exercise routine and access to a social media page to facilitate social support and interaction among the group participants. Participants will be able to join the group if they would like, but it will not be required. Participants will be encouraged to connect with each other to promote social support and social modeling. Lastly participants will receive a weekly exercise video to follow along with on their own time and tailored weekly step goals.
Educational Comparison Group
ACTIVE COMPARATORThe education group participants will receive the same exercise manual, fitness items, exercise videos, and same weekly tailored step goal as the 12-week intervention group. This group will not have weekly zoom discussions, or be a part of the same social media page as the 12-week intervention group. Instead, the education group will be contacted by research staff once a week via telephone to discuss their manuals and activity for the week, and to ensure they have been safely engaging in exercise. A separate social media page will be created for this group, where pre-existing materials related to physical activity recommendations, benefits, other resources, and more will be shared.
Interventions
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
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Illinois at Urbana-Champaign
Urbana, Illinois, 61801, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Neha P Gothe, MA, PhD
University of Illinois at Urbana-Champaign
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 23, 2020
First Posted
August 4, 2020
Study Start
October 2, 2021
Primary Completion
December 31, 2022
Study Completion
December 31, 2022
Last Updated
January 31, 2023
Record last verified: 2023-01