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To find the effect of Virtual reality on shoulder pain and movement after mastectomy in breast cancer survivors.

Effect of Virtual Reality-Based Upper Limb Rehabilitation on shoulder pain, range of motion, strength, fear of movement and upper limb function in post mastectomy Breast cancer survivors: A Randomised Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108209
Enrollment
40
Registered
2026-04-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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: Effect of Virtual Reality-Based Upper Limb Rehabilitation on shoulder pain, range of motion, strength, fear of movement and upper limb function in post mastectomy Breast cancer survivor

Sponsors

Shavni sunil Banaulikar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed with breast cancer post mastectomy within 2 to 8 weeks Age between 18 and 70 years Presence of shoulder dysfunction MMSE score 24 or more Able to follow instructions Willing to participate

Exclusion criteria

Exclusion criteria: Metastatic disease or unstable medical condition Severe post operative complications Vestibular disorders or seizures Claustrophobia or intolerance to virtual reality Skin conditions preventing use of VR

Design outcomes

Primary

MeasureTime frame
1. Pain severity VAS ( visual analogue scale ) 2.Shoulder Range of Motion (ROM) Measured using goniometer. Flexion, abduction and external rotation 3.Muscle Strength measured by MMT or handheld dynamometer. 4.Fear of Movement (Kinesiophobia) Tampa Scale of Kinesiophobia. 5.Upper Limb Function QuickDASH score (Disabilities of Arm, Shoulder and Hand) Timepoint: Baseline 0 weeks 4 weeks follow up 8 weeks—

Secondary

MeasureTime frame
Mini-Mental State Examination (MMSE) to assess cognitive functionTimepoint: Baseline 0 weeks—

Countries

India

Contacts

Public ContactShavni Sunil Banaulikar

GOA MEDICAL COLLEGE AND HOSPITAL

pamela.dsilva@ymail.com7353594793

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026