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Using Virtual Reality to Reduce Pain and Swelling in Breast Cancer Survivors

Efficacy of Virtual Reality Based Lymphatic Intervention on Pain, Swelling among Breast Cancer Survivors - Nil

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072753
Enrollment
30
Registered
2024-08-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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: VR exercise intervention: Protocol : 3days per week for 4 week/ 1month 10mins per session for 1 day Control Intervention1: NIL: NIL

Sponsors

MOHAMED ANAS A
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Only Women Age: 40 to 50 years Mastectomy – Simple and Modified Radical Stages II & III Duration -2 months old Mini mental status examination score greater than 25 Willing to participate

Exclusion criteria

Exclusion criteria: Severe chronic conditions Spider web syndrome Compression garments Allergies or skin conditions

Design outcomes

Primary

MeasureTime frame
1. Perceived Ease of Use and Usefulness Questionnaire 2. Breast Cancer and Lymphedema Symptom Experience Index (BCLE - SEI)Timepoint: 20 minutes—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactSURESH J

SRM College of Physiotherapy

sureshj@srmist.edu.in9698642928

Outcome results

None listed

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