Clinical trial · Interventional
Consciousness-based Ayurveda Lifestyle Program for Improving Quality of Life in Survivors of Breast Cancer
Evaluation of an Ayurvedic Whole Systems-based Lifestyle Protocol for Quality of Breast Cancer Survivorship: A Randomized Controlled Pilot Study
NCT05743023CI-TRIAL-00064238unknownN/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 a pilot study to assess the feasibility and effectiveness of a 12-week intervention of personalized diet and lifestyle protocol based on the principles of Ayurveda's whole systems approach to achieving improvement in a) quality of life, b) digestive health, c) sleep among women breast 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 |
|---|---|---|---|
| Breast Cancer Survivors | Breast Neoplasm | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Ayurvedic lifestyle protocol | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Consciousness-based Ayurvedic lifestyle Intervention
- description
- In the intervention group, each participant will receive a structured education and be asked to follow a 12-week personalized diet and daily routine protocol based on the assessment of their current Ayurvedic mind-body state. Participants will be asked to complete the self-reported questionnaires at baseline, 6, and 12-week.
- interventionNames
- Behavioral: Ayurvedic lifestyle protocol
- type
- ACTIVE_COMPARATOR
- label
- Waitlist control
- description
- Participants in the waitlist control group will not receive any intervention. They will continue usual care and will be asked to complete the self-reported questionnaires at baseline, 6, and 12-week. Participants n this group receive their personalized protocol at the end of 12 weeks after completing all the data collection.
- interventionNames
- Behavioral: Ayurvedic lifestyle protocol
Primary outcomes (3)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * A breast cancer survivor in remission (Females ≥ 18 years) * Diagnosis of stage I-IV breast cancer * Three months or more after receiving conventional treatment (chemotherapy, radiation therapy, and/or surgery) * Willing to comply with the study intervention recommendations for 12 weeks * English speaking * Have access to technology to participate in zoom visits Exclusion Criteria: * Male responders * Inability to provide informed consent * Physiological or psychological debility that would interfere with the ability to participate in the study fully * Active metastatic or recurrent disease (to avoid early withdrawal from the study) * Anticipates undergoing surgery during the duration of the intervention * Substance abuse (to avoid early withdrawal from the study)
References
Publications (0)
Data not yet available
No reference posted for this study.