Clinical trial · Interventional
Mila Blooms Intervention Study
Mila Blooms Intervention Study: An App for Promoting Physical Activity and Health Diet Among Adolescent Survivors of Childhood Cancer
NCT01473342CI-TRIAL-00015895completedN/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)
This study is focused on the development and pilot/feasibility testing of a smartphone application to promote a healthy diet, increase physical activity, and prevent weight gain in adolescent survivors of childhood cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Childhood Cancer | Childhood Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Mila Blooms | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Control & Intervention Phases
- description
- The control phase will run for 8 weeks, including survey completion and accelerometer wear during Week 1 and Week 8. The intervention phase will run for the 9 weeks following the control phase; where participants are assigned a smartphone to interact with the Mila Blooms gaming app and integrated social network \& receive weekly supportive coaching phone calls from study staff for 8 weeks (Week 9 - Week 16) followed by accelerometer wear \& survey completion during the 9th and final week (Week 17).
- interventionNames
- Behavioral: Mila Blooms
Primary outcomes (1)
- measure
- Feasibility of the Mila Blooms Intervention at changing health behaviors.
- timeFrame
- ~9 weeks (from pre-intervention baseline to post-intervention follow-up)
- description
- Test the feasibility of the Mila Blooms intervention at changing diet, physical activity, body mass index (BMI), and social cognitive mediators of health behavior change.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 12 Years
- Maximum age
- 19 Years
Show eligibility criteria text
Inclusion Criteria: * Participants must speak \& read/write fluent English; * Adolescent must be between 12 and 19 years of age; * Adolescent must have a previous diagnosis of childhood Acute Lymphoblastic Leukemia; * Adolescent must be "off-therapy" (i.e., not in active or maintenance phase of cancer therapy) for at least 2 years; * Adolescent must be cleared by his/her physician to participate (defined by obtaining a score of 80 or greater on the Karnofsky Scale as determined by their physician); * Participants must have a working phone number; * Adolescents must live at home with parents in order to facilitate parent involvement via support materials. Exclusion Criteria: * Physician reports that the patient has deficits in neurocognitive functioning that would preclude him/her from participating in a cognitive-oriented intervention;
References
Publications (0)
Data not yet available
No reference posted for this study.