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Clinical Trials/NCT06553183
NCT06553183
Not yet recruiting
Not Applicable

Immersive Virtual Reality Based Exersice and Shoulder Proprioception and Range of Motion in Post-mastectomy Lymphedema Patients

Cairo University0 sites60 target enrollmentStarted: August 15, 2024Last updated:
ConditionsLymphedema Arm

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
60
Primary Endpoint
shoulder proprioception

Overview

Brief Summary

To determine the effect of immersive virtual reality on shoulder proprioception and ROM of post-mastectomy lymphedema patients.

Detailed Description

RESEARCH QUESTION:

Does Immersive virtual reality based exercise effective in improving shoulder proprioception and ROM for post-mastectomy patients?

Assessment:

The digital goniometer will be used in measuring shoulder extension, flexion, adduction, abduction, internal rotation and external rotation before the sessions and after one month of sessions. Also, shoulder proprioception will be assessed by the digital goniometer.The measurement will be taken for both the edematous side and the non-affected side.

Treatment:

Study group: the patients will receive eight sessions of Immersive virtual reality based exercise, 2 sessions per week for 4 weeks besides the traditional physical therapy.

Control group: the patients will receive eight sessions of the traditional physical therapy, 2 sessions per week for 4 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
35 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All the patients will be females.
  • Patients with lymph node dissection.
  • start at least 2 weeks after operation.

Exclusion Criteria

  • Vision problems.
  • Medically instable patients.
  • Balance disorders.
  • Other musculoskeletal condition of shoulders.

Outcomes

Primary Outcomes

shoulder proprioception

Time Frame: 4 weeks

digital goniometer

Secondary Outcomes

  • shoulder ROM(4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

doaa atef

lecturer of physical therapy for surgery

Cairo University

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