The Impact of Innovative Technology Strategies on Implementing Exercise Programs Using Fully Immersive Virtual Reality for Postpartum Women

NCT05921747 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2026-04-13

No results posted yet for this study

Summary

The study aims to determine the effect of traditional exercise through using fully immersive virtual reality in postpartum female with lumbopelvic pain.

This study will be single-blind randomized clinical -trial and will be conducted at Shalamar Institute of health sciences in 1 year after the approval by institutional review board. Sixty female participants with a history of lumbopelvic pain will be recruited on the basis of inclusion and exclusion criteria. Data will be collected after taking written Informed Consent from each patient. The included participants will be randomized by gold fish randomization method and allocated to two groups (A \& B) each with 30 participants.

Conditions

  • Post Partum Lumbopelvic Pain

Interventions

OTHER

Traditional exercise as control group

Standard Traditional exercise program: The traditional exercises will include Kegel pelvic floor exercise, dead weight lifts, wide back rows, lunges with rotation, good morning (hip hinge), and lateral side bends. . Pre and post measurement will be taken before and after the session.

DEVICE

VR Intervention Group Protocol

Participants in the intervention group will undergo a virtual reality (VR)-based exercise program using Meta Quest 2 head-mounted displays (Meta Platforms Inc., USA) and the Lumbar Pain Rehab software provided by DynamicsVR (Dynamics VR S.L., Cadiz, Spain). The virtual reality (VR) intervention will consist of eight structured sessions designed to address postpartum lumbo-pelvic pain through the immersive, interactive training. Each session incorporating pelvic floor muscle training using VR, consisting of three sets of 12 repetitions, with each contraction and relaxation phase lasting three seconds. In addition, patients engaged in two five-minute blocks of immersive VR activities with a two-minute rest interval, resulting in total session duration of 18 minutes. A familiarization session will be conducted prior to the intervention to acclimate participants to the VR environment. This will include modified pelvic floor training (3 sets of 8 repetitions; 3 seconds of contraction.

Sponsors & Collaborators

  • Shalamar Institute of Health Sciences

    lead OTHER

Principal Investigators

  • Javeria Dr Aslam, Ph.D · Shalamar Institute of Health Sciences

  • Carlos R. Morales, Ph.D · Universided Europea Madrid, Spain

  • RAQUEL DIAZ-MECO, Ph.D · Universided Europea Madrid, Spain

  • Alba P. Alemany, Ph.D · Department of Radiology & Physical Medicine, Complutense University of Madrid, Spain

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-02
Primary Completion
2026-03-31
Completion
2026-04-30

Countries

  • Pakistan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05921747 on ClinicalTrials.gov