Clinical trial · Interventional
Move Together Boston Feasibility Pilot (Sit Less, Move More App for Black Breast Cancer Survivors & At-Risk Relatives)
"Sitting Less, Moving More": Designing a Digital Health Intervention for Black and African American Women Breast Cancer Survivors and Their At-risk Relatives (Phase II)
NCT05011279CI-TRIAL-00071373completedN/AResults postedClinicalTrials.gov clinicaltrialsProvenance
- 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 purpose of this study is to develop and test a mobile app for Black/African American breast cancer survivors and their relatives, called Move Together, that promotes sitting less and moving more for better health.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Breast Cancer Survivor | Breast Neoplasm | PROBABILISTIC | 0.70 |
| Fitness Trackers | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Move Together app/Garmin Activity Tracker | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Pilot Study
- description
- Participants in the pilot study will participate as members of family-based dyads (n=5 dyads). One member of each dyad will be a breast cancer survivor and one will be a blood relative. Study involves interviews, questionnaires, Use of Move Together app with Garmin activity tracker watch
- interventionNames
- Other: Move Together app/Garmin Activity Tracker
Primary outcomes (1)
- measure
- System Usability Scale (SUS) Score
- timeFrame
- Assessed at 4 Weeks
- description
- The acceptability of the Move Together app will also be assessed with The System Usability Scale (SUS) score. The scale has 10 items. Scores range from 0-100; a SUS score above a 68 is considered above average (https://www.usability.gov/how-to-and-tools/methods/system-usability-scale.html.)
Secondary outcomes (7)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * 1a) Key informants (for interviews) * Members of the community/advisory groups, community health centers, or faith-based network members (e.g., Pink and Black, Faces of Faith). * English speaking adults. * (1b) Breast cancer survivors and relatives (for interviews) * Self-identify as Black or African American * Age 18 and over * English speaking * Female breast cancer survivor status post curative antineoplastic treatment (except ongoing hormonal treatment) with no evidence of disease, OR a first degree blood relative (parent, child, or full sibling), of any gender, of a so defined breast cancer survivor * Self-report ever using a smart phone * (2) Breast cancer survivors and relatives (for user testing/interviews) * Self-identify as Black or African American * Age 18 and over * English speaking * Female breast cancer survivor status post curative antineoplastic treatment (except ongoing hormonal treatment) with no evidence of disease, OR a first degree blood relative (parent, child, or full sibling), of any gender, of a so defined breast cancer survivor * Self-report willing/able to download the app for testing on a smart phone * Self-report willing/able to meet via Zoom for interview * (3) Breast cancer survivors and relatives/"buddies" (for pilot testing) * Self-identify as Black or African American * Age 18 and over * English speaking * Breast cancer survivor status post curative antineoplastic treatment (except ongoing hormonal treatment) with no evidence of disease, OR a blood relative, of any gender, of a so defined breast cancer survivor * Self-report willing/able to participate with a blood relative in survivor relative dyad * Self-report willing/able to download the app for use on a smart phone * Self-report willing/able to meet via Zoom for instructions and interview Exclusion Criteria: * (1a) Key informants (for interviews) --None * (1b) Breast cancer survivors and relatives (for interviews) * Requires medically supervised physical activity (Physical Activity Readiness Question for Everyone, PAR-Q+, Question 7) * Pregnant women * (2) Breast cancer survivors and relatives (for user testing/interviews) * Requires medically supervised physical activity (Physical Activity Readiness Question for Everyone, PAR-Q+, Question 7) * Pregnant women * (3) Breast cancer survivors and relatives/"buddies" (for pilot testing) * Meets exclusion criterion of the Modified Physical Activity Readiness Questionnaire (PAR-Q) (modified) * Participated in interviews or user testing in prior phases of the study
References
Publications (1)
- DERIVEDBlazey M, Marinac C, Whiteley J, Peterson S, Burns White K, Jacques C, Lam H, Halpenny B, Patel S, Lamothe R, Wright J. Designing a Dyad-Based Digital Health Intervention to Reduce Sedentary Time in Black Breast Cancer Survivors and Their First-degree Relatives: Human-Centered Design Study. JMIR Form Res. 2023 May 24;7:e43592. doi: 10.2196/43592. PMID 37223968