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| Name | Class |
|---|---|
| University of Colorado, Denver | OTHER |
| Brown University | OTHER |
| InquisitHealth, Inc. | OTHER |
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This is a 3-month physical activity intervention aimed to increase moderate-intensity activity among previously inactive breast cancer survivors. Participants will be eligible if they are not currently active, and have recently been diagnosed with breast cancer. Upon eligibility, participants will be randomized into one of two groups. The intervention group will receive weekly guidance from a peer coach to increase their activity throughout the three month intervention. The control group will be encouraged to self-monitor their physical activity throughout the three month intervention. Both groups will receive a Fitbit. Peer coaches will be trained to deliver the physical activity program using a web-based platform; all calls will be virtual. Participants will be assessed before and after the intervention.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| webMFT | Experimental | Survivors randomized to webMFT will receive the evidence-based intervention for moderate-to-vigorous physical activity (MVPA) promotion that consists of MVPA counseling matched to patients' motivational readiness, and self-monitoring of MVPA (via Fitbit Inspire 2). The goal for the 3-month program will be to gradually increase the amount of moderate-intensity aerobic exercise that is performed, to the current national recommendations of at least 150 minutes of MPVA per week. Our goal is to promote aerobic exercise that is safe and enjoyable, such as walking. |
|
| MVPA tracking | Active Comparator | These survivors will be asked to self-monitor moderate-to-vigorous physical activity (MVPA) participation by wearing the Fitbit Inspire 2 each day over 12 weeks. This group will not receive the MVPA counseling from the coaches. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Physical activity adoption | Behavioral | webMFT will be delivered via a web-based platform. Coaches will be trained to deliver the intervention prior to being assigned a study participant. Upon successful completion of the informed consent for coaches and participants, coaches will be assigned a participant for their 3-month duration in the study. Coaches and participants will complete weekly phone calls focused on increasing the participants' MVPA up to the recommended 150 min/week. |
| Measure | Description | Time Frame |
|---|---|---|
| Accelerometer measured moderate-to-vigorous activity | Minutes of moderate-to-vigorous intensity activity at 3-month follow-up | 3-month intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Self-Reported Quality of Life | Assessed via FACT-B, validated questionnaire | Pre-intervention and post 3-month intervention |
| Self-Reported Physical Functioning | Assessed via SF-36, validated questionnaire |
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Participants:
Inclusion Criteria:
Exclusion Criteria:
Peer Mentor Coaches:
Inclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Bernardine M. Pinto, PhD | University of South Carolina | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of South Carolina | Columbia | South Carolina | 29208 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 41005365 | Derived | Ostendorf DM, Huebschmann AG, Wickersham KE, Kindred M, Pinto BM. Adopting and implementing an efficacious peer-delivered physical activity program for web platform delivery in survivors of breast cancer: organizational readiness and perspectives. Transl Behav Med. 2025 Jan 16;15(1):ibaf051. doi: 10.1093/tbm/ibaf051. | |
| 40423894 | Derived |
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Data can be shared upon request.
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| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| D057185 | Sedentary Behavior |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
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| ID | Term |
|---|---|
| D015190 | Blood Glucose Self-Monitoring |
| ID | Term |
|---|---|
| D001774 | Blood Chemical Analysis |
| D019963 | Clinical Chemistry Tests |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
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This is a randomized controlled trial. Participants will be randomly assigned to a intervention group or a control group. The study duration will be 3-months for both groups; assessments will be completed pre- and post-intervention.
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| Self monitoring | Behavioral | Participants will be asked to gradually increase their activity up to the recommended 150 minutes of moderate-intensity/week during the 12-week intervention. Self-monitoring will be completed using a Fitbit tracker. |
|
| Pre-intervention and post 3-month intervention |
| Self-Reported Mood | Assessed via Profile of Mood States, validated questionnaire | Pre-intervention and post 3-month intervention |
| Self-Reported Fatigue | Assessed via FACIT-F, validated questionnaire | Pre-intervention and post 3-month intervention |
| Pinto BM, Kindred M, Dunsiger S, Mitchell S, Patel A, Ostendorf D, Huebschmann AG. Effects of web platform delivery of a physical activity program for breast cancer survivors: a randomized controlled trial. J Cancer Surviv. 2025 May 27. doi: 10.1007/s11764-025-01811-7. Online ahead of print. |
| 38896452 | Derived | Pinto BM, Patel A, Ostendorf DM, Huebschmann AG, Dunsiger SI, Kindred MM. Adapting an Efficacious Peer-Delivered Physical Activity Program for Survivors of Breast Cancer for Web Platform Delivery: Protocol for a 2-Phase Study. JMIR Res Protoc. 2024 Jun 19;13:e52494. doi: 10.2196/52494. |
| D017437 |
| Skin and Connective Tissue Diseases |
| D001519 | Behavior |
| D003933 | Diagnosis |
| D003940 | Diagnostic Techniques, Endocrine |
| D008991 | Monitoring, Physiologic |
| D000085263 | Self-Testing |
| D012648 | Self Care |
| D013812 | Therapeutics |
| D008919 | Investigative Techniques |