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Immersive Virtual Reality Based Exersice in Post-mastectomy Lymphedema Patients

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

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06553183
Enrollment
60
Registered
2024-08-14
Start date
2024-08-15
Completion date
2025-02-15
Last updated
2024-08-14

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

Conditions

Lymphedema Arm

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.

Interventions

PROCEDUREimmersive virtual reality

Exercise based on virtual reality video games. Immersive type will be used.

PROCEDUREtraditional physicaltherapy

pneumatic compression, exercise and skin care

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
35 Years to 65 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
shoulder proprioception4 weeksdigital goniometer

Secondary

MeasureTime frameDescription
shoulder ROM4 weeksall 6 motions will be measured by digital goniometer

Contacts

Primary Contactdoaa atef, PhD
doozy.masr@gmail.com+201060267094

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026