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Effect of Pressure Biofeedback Training After Ventral Hernioplasty

NCT07642219 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2026-06-11

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the effect of pressure biofeedback training on abdominal muscle strength and quality of life in adults following ventral hernioplasty. The main questions it aims to answer are:

* Is there a significant effect of pressure biofeedback training on abdominal muscle strength in patients following ventral hernioplasty?
* Is there a significant effect of pressure biofeedback training on quality of life in patients following ventral hernioplasty?

Researchers will compare the effect of adding pressure biofeedback training to a conventional physical therapy program versus a conventional physical therapy program alone to determine whether pressure biofeedback training provides additional benefits in improving abdominal muscle strength and quality of life following ventral hernioplasty.

Participants in the study group will receive pressure biofeedback training in addition to the conventional physical therapy program, while participants in the control group will receive the conventional physical therapy program only.

Conditions

  • Ventral Hernia Repair

Interventions

OTHER

pressure biofeedback training

participants in study group will receive 30 mins and 3 sessions per week for 8 weeks

OTHER

conventional physical therapy program

A conventional physical therapy program will include abdominal muscle strengthening without pressure biofeedback device.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
35 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-06
Primary Completion
2026-04-30
Completion
2026-04-30

Countries

  • Egypt

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 NCT07642219 on ClinicalTrials.gov