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To study the effect of Yoga Practices on Quality of Life, Mental Health, Treatment-related Symptoms, and Ayurvedic Classification of Prakruti, Vikruti in Breast Cancer Patients Undergoing Radiotherapy

Effect of Integrative Yoga Program on Quality of Life, Mental Health, Prakriti, and Treatment-related Symptoms in Breast Cancer Patients Undergoing Radiotherapy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098469
Enrollment
128
Registered
2025-12-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C50- Malignant neoplasm of breast Health Condition 2: D- Radiation Therapy

Interventions

Intervention1: Conventional Radiation Therapy +Integrative Yoga: Radiation Schedule + Integrative yoga. Duration 12 weeks, Length of session 30-45 minutes and practices - Prakruti related Life-style +

Sponsors

Dr Sunita Chaudhari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects with a confirmed diagnosis of Breast cancer patients, stage I to III, scheduled to undergo radiotherapy, ECOG-PS: 0 to 2 or KPS score more than 70, who are willing to give consent and participate in the 12-week intervention study protocol for hybrid-online and offline mode

Exclusion criteria

Exclusion criteria: Subjects with Stage IV breast cancer with Metastasis, Patient planned for Brachytherapy, Neo-adjuvant Chemo with radiotherapy, currently doing another form of structured yoga, Severe medical co-morbidities, inability to perform yoga, Pregnant women, those who are on medication for severe psychotic diseases, Severe immobility due to arthritis, vision, and hearing impairment

Design outcomes

Primary

MeasureTime frame
EORTC 42 (Quality of life), HADS (Anxiety and Depression Score), PSS (Perceived Stress score), PSQI (Pittsburgh Sleep Quality score), treatment-related symptoms(VAS Score), Prakruti -vikruti questionnaire, Nadipariksha score Timepoint: Timepoints: T1=Baseline (prior to start of radiation therapy) T2= End of radiation therapy (approx. 6 weeks from baseline) T3= 12 weeks from baseline EORTC 42:T1.T2,T3, HADS:T1.T2,T3, PSS:T1,T2,T3, PSQI:T1T2T3, symptoms(VAS Score): T1,T2,T3, Prakruti -vikruti Priksha: T1,T2 Nadipariksha: daily between T1 and T2

Secondary

MeasureTime frame
Hear Rate Variability (HRV )Timepoint: T1,T2

Countries

India

Contacts

Public ContactDr Sunita Chaudhari

Dr.Vishwanath Karad MIT World Peace University

sanjeev.kumar@mitwpu.edu.in09850060068

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026