Clinical trial · Interventional
Mobile Behavior Change Program for Weight Loss in Breast Cancer Survivors
Preliminary Examination of a Mobile Behavior Change Program for Weight Loss in Breast Cancer Survivors
NCT04753268CI-TRIAL-00061286completedN/AClinicalTrials.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 evaluate the preliminary efficacy of a Noom Breast Cancer Weight Loss Program on weight loss outcomes, quality of life, and physical activity. Also, to qualitatively determine acceptability of this novel program among breast cancer survivors with overweight or obesity.
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 |
|---|---|---|---|
| Behavior, Health | — | UNRESOLVED | — |
| Weight Loss | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Noom Healthy Weight Program | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment group: Noom Healthy Weight Program
- description
- The intervention consists of a curriculum, provided through daily articles that users are encouraged to read; logging features for weight, meals, and physical activity; in-app groups; and a virtual coach, who will communicate with participants via in-app messaging.
- interventionNames
- Behavioral: Noom Healthy Weight Program
Primary outcomes (4)
- measure
- Weight
- timeFrame
- baseline to 6 months
- description
- Self-reported weight
- measure
- Program engagement
- timeFrame
- weeks 1-26
- description
- Engagement with the Noom program; measured as 1. Number of App opens 2. Messages to coach 3. Number of Steps 4. Logged food 5. Logged exercise 6. Group messages and likes 7. Articles read
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Able to understand and provide informed consent * 18 years and older * Overweight or obesity (BMI ≥ 27.5) * Not 6 months postpartum * Not planning to become pregnant in the next 7 months * Have a smartphone that is compatible with Noom's mobile app * Breast cancer survivor with stage I, II, or III * Completed active treatment (e.g, surgery, chemo, radiation, etc.) \> 6 months ago Exclusion Criteria: * Inability or unwillingness of a participant to give written informed consent * Currently pregnant or \< 6 months postpartum * Plans to become pregnant within the next 7 months * Stage IV, metastatic cancer or DCIS * Currently taking insulin * Uncontrolled hypertension
References
Publications (1)
- DERIVEDShen S, Salehi E, White C, Chen Y, Iyengar NM. Evaluation of a mobile behavior change program for weight loss in breast cancer survivors. NPJ Breast Cancer. 2024 Jun 29;10(1):53. doi: 10.1038/s41523-024-00659-x. PMID 38951532