Clinical trial · Interventional
Feasibility, Acceptability, and Preliminary Efficacy of a Remotely-delivered Health Coaching Intervention for Cancer Survivors
NCT07026214CI-TRIAL-00091121completedN/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 aimed to evaluate the feasibility, acceptability, and preliminary efficacy of an 8-week, remotely delivered health coaching intervention designed to improve: 1) targeted psychosocial mechanisms of action (behavioral regulation skills, affective attitudes, health habits, and identity); 2) health behaviors (physical activity, diet, sleep); and 3) cancer-related health outcomes (physical function, anxiety, depression, fatigue, and pain) among young and middle-aged adult cancer survivors.
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 |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Vitalis Cancer | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Vitalis Cancer Intervention
- description
- The intervention includes health coaching, health education, and wearable activity monitoring.
- interventionNames
- Behavioral: Vitalis Cancer
Primary outcomes (4)
- measure
- Feasibility - Enrollment
- timeFrame
- From the first day of study recruitment until the date of the last participant to complete the intervention, assessed up to 36 months
- description
- Enrollment rates calculated as percentage of enrolled vs interested participants
- measure
- Acceptability
- timeFrame
- Post-intervention (8 weeks)
- description
- Participants self-reported their acceptability with each intervention feature using an Acceptability Survey. Responses were collected using a 5 point likert scale with higher numbers representing greater satisfaction (1=Very disatisfied, 5=Very Satisfied)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: * Adult cancer survivors aged 18-64 years * 3-60 months post-treatment * Not meeting recommendations for physical activity, diet, or sleep. * Express interest in improving at least one health behavior. Exclusion Criteria: * Currently receiving cancer treatment * Metastatic disease * Pregnancy or plans for pregnancy * No access to Zoom or a smartphone
References
Publications (0)
Data not yet available
No reference posted for this study.