Skip to content

EFFECT OF STRUCTURED PHYSICAL THERAPY INTERVENTION VERSUS CONVENTIONAL THERAPY IN PATIENTS WITH MODIFIED RADICAL MASTECTOMY

EFFECTIVENESS OF STRUCTURED PHYSICAL THERAPY INTERVENTION VERSUS CONVENTIONAL THERAPY ON SHOULDER DYSFUNCTION, QUALITY OF LIFE AND FATIGUE LEVEL IN PATIENTS WITH MODIFIED RADICAL MASTECTOMY IN A RURAL SETUP- A RANDOMIZED CONTROLLED TRIAL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042930
Enrollment
100
Registered
2022-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: Experimental Group: Day 1 to Week 2 Breathing Exercises â?? Pursed Lip Breathing and Diaphragmatic Breathing â?? 4-5 times/day each 2 sets with 10 breaths/set, Progression in week 2 Pur

Sponsors

DR APJ ABDUL KALAM COLLEGE OF PHYSIOTHERAPY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women more than 18 years age Clinically diagnosed with breast cancer according to imaging and pathological examination. Surgical treatment of breast includes modified radical mastectomy, Mastectomy, or conservation surgery. Pain VAS score more than 1 Patient willing to participate and giving informed consent.

Exclusion criteria

Exclusion criteria: Patients with severe deformity, any trauma or diseases affecting muscles and joints such as Rheumatoid Arthritis, skin grafting on or around the shoulder. Previous chronic illness such as diabetes, osteoporosis, renal failure, heart disease. Neurological dysfunction. Patients undergone Recent Shoulder surgery

Design outcomes

Primary

MeasureTime frame
Shoulder Range of Motion strength pain Quality of Life Fatigue Level Timepoint: The data will be collected at baseline, 2 week, 4 week, 6 week and follow up

Secondary

MeasureTime frame
1. Endurance -6 MWT 2. BMI 3. Body fat % Omron HBF-375 Body Composition Monitor Timepoint: The data will be collected at baseline, 2 week, 4 week, 6 week and follow up

Countries

India

Contacts

Public ContactDR ADITI PRAMOD KHOT PhD Scholar

DR. BALASHAHEB VIKHE PATIL RURAL MEDICAL COLLEGE

vaiphalke@gmail.com9822840790

Outcome results

None listed

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