Clinical trial · Interventional
Survivor mHealth: Wearable Devices in Cancer Survivors
Survivor mHealth: Assessing Feasibility of a Wearable Device and App in Cancer Survivors
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The Survivor mobile health (mHealth) study is testing the use of wearable devices (Fitbits) and a smartphone application in cancer survivors. The goal of the program is to increase survivor's physical activity levels. The Fitbit will be synced to the app and participants will receive messages and notifications about their activity levels. Participants will also complete surveys through the app asking how useful it is and ways to improve it. The study team will conduct qualitative interviews at the completion of the 3 months to see how participants liked the program, and ways it can be improved and make it more specific to cancer survivors. The study team will also conduct interviews with providers and clinic staff to assess their perceptions of patient digital health programs and preferences for receiving patient-generated health data.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
| Cardiovascular Diseases | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Wearable device deployment | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Wearable device deployment
- description
- Participants will be enrolled in the experimental trial to receive Fitbits and a smartphone app.
- interventionNames
- Behavioral: Wearable device deployment
Primary outcomes (1)
- measure
- Feasibility of Enrollment
- timeFrame
- Baseline
- description
- Feasibility will be determined by a participant meeting all three criteria: 1) Enrollment in trial, 2) completion of baseline measures, and 3) Fitbit sync to app.
Secondary outcomes (2)
- measure
- 3-month Daily Step Count
- timeFrame
- At study completion, within 3-months of enrollment
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 100 Years
Show eligibility criteria text
Aims 1 and 2 Inclusion Criteria: 1. Past cancer diagnosis 2. At least 18 years of age 3. Capacity to provide informed consent 4. Medically cleared to perform physical activity (as noted by Physical Activity Readiness Questionnaire form or physician's clearance if needed) 5. Owns a smartphone Aims 1 and 2 Exclusion Criteria: 1. Is a prisoner 2. Non-English speaking 3. Is unable to provide consent 4. Under 18 years of age 5. No prior cancer diagnosis 6. Does not own a smartphone Aim 3 Inclusion Criteria: 1. Are a current UMass Memorial Cancer Clinic patient navigator, oncologist, radiologist, or cardiologist 2. Consent to participate Aim 3 Exclusion Criteria: 1. Not currently employed at UMass Memorial 2. Not involved in direct treatment of care coordination of cancer patients
References
Publications (0)
Data not yet available