Clinical trial · Observational
Reborn Lifestyle Adjustment Program
Reborn Lifestyle Adjustment Program for Breast Cancer Patients
NCT06608043CI-TRIAL-00080957unknownClinicalTrials.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 aim of this study is to investigate the effects of the reborn lifestyle regulation program on physical activity, fatigue level, pain, mental health burden and quality of life in breast cancer patients.
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 |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Quality of Life | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Conventional Physiotherapy and Occupational Therapy | Procedure | — | UNRESOLVED |
| Reborn lifestyle adjustment program | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Intervention Group
- description
- This intervention group consists of multi-component modules developed to help individuals with breast cancer adopt a healthy lifestyle and improve their quality of life. The sessions are based on the 'Do Live Well' model, Kolb's Experiential Learning Theory, and CBT-based problem-solving skills.
- interventionNames
- Behavioral: Reborn lifestyle adjustment program
- label
- Control Group
- description
- Patients in the control group will continue conventional medical treatments, occupational therapy and physiotherapy sessions.
- interventionNames
- Procedure: Conventional Physiotherapy and Occupational Therapy
Primary outcomes (7)
- measure
- Breast Cancer Specific Quality of Life Scale
- timeFrame
- 12 weeks
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Being a female individual aged 18 or older * Have been diagnosed with Stage I, II, or III breast cancer * At least 6 months have passed since the completion of chemotherapy * Approval by an oncologist to participate in the study * Having internet access and the ability to connect online * Scoring above 23 on a standardized Mini Mental Status Examination Test * Being in the contemplation stage according to the Transtheoretical Model Exclusion Criteria: * Having a neurological or systemic disease that could significantly affect the course of the intervention * Having metastasis that could impact the sustainability of the study * Suffering from neuropathic pain * Having participated in a healthy lifestyle program within the last 3 months
References
Publications (0)
Data not yet available
No reference posted for this study.