NCT07237776

Brief Summary

Cesarean section is mainly performed using regional anesthesia, without preoperative sedatives, to facilitate the mother's conscious birth experience, reduce the need for neonatal resuscitation, and promote skin-to-skin contact immediately after birth between the mother and newborn. The VR can be designed to be an interacting and emotionally engaging environment that can stimulate emotionally related hormones. In stressful situations as CS, VR can generate a relaxation state that improves the surgery outcomes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 20, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 2, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

August 28, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

November 20, 2025

Completed
Last Updated

November 20, 2025

Status Verified

November 1, 2025

Enrollment Period

5 months

First QC Date

August 28, 2025

Last Update Submit

November 18, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • hand held dynamometer

    isokinetic dynamometer hand held dynamometer hand held dynamometer used to measure the abdominal muscle strength, endurance and fatidue

    2 month

Secondary Outcomes (1)

  • rectus diastasis test

    2 month

Study Arms (2)

virtual reality group

EXPERIMENTAL

using virtual reality technology to perform abdominal muscle training 3 sessions per week for eight weeks

Device: Virtual reality Glasses

Active Abdominal exercise group

EXPERIMENTAL

abdominal muscle training using Active Abdominal exercises 3 sessions per week for eight weeks.

Other: active abdominal exercises

Interventions

Virtual reality Glasses (is an advanced, standalone virtual reality (VR) headset that delivers a fully immersive experience without reliance on external hardware such as a PC, gaming console, or external tracking sensors. It utilizes an integrated inside-out tracking system that enables users to move freely within their physical environment while maintaining accurate spatial orientation. The device incorporates high-resolution displays, a high-performance processor, and ergonomically designed controllers that enhance interactivity and user engagement within virtual environments

virtual reality group

Trunk flexion refers to bending the spine forward, mainly activating the rectus abdominis (the "six-pack" muscle). This movement is commonly seen in crunches or sit-ups. Straight Leg Raise (SLR) is a movement that strengthens the lower abdominal muscles and hip flexors. It involves raising the legs while keeping them straight, without bending at the knees. both exercises were done with 30 reptations (3 sessions per week for 8 weeks)

Active Abdominal exercise group

Eligibility Criteria

Age25 Years - 35 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsproblem is cesarean section which is happening in females only
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • female from 25 to 35 years
  • post cesarean section

You may not qualify if:

  • neurological problems
  • musculoskeletal disorders

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo university

Cairo, 11411, Egypt

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
single blind participant
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized control trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

August 28, 2025

First Posted

November 20, 2025

Study Start

October 20, 2024

Primary Completion

April 2, 2025

Study Completion

July 20, 2025

Last Updated

November 20, 2025

Record last verified: 2025-11

Locations