Chest Physiotherapy and Aerobic Training in Children Post Abdominal Surgery

October 22, 2024 updated by: Vandana Esht, University of Jazan

Effects of Chest Physiotherapy and Aerobic Exercise Training in Improving Physical Fitness InYoung Children Post Abdominal Surgery: an Experimental Trial

This study will underscore the clinical importance of integrating chest physiotherapy and aerobic exercise training into the post-abdominal surgery care regimen for young children.By improving physical fitness levels, these interventions contribute significantly to the overall recovery process and enhance the well-being of pediatric patients. Implementing such strategies can optimize functional outcomes, reduce complications, and promote a faster return to normal activities, thereby improving the quality of life for young patients undergoing abdominal surgery.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

23

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Uttaranchal
      • Roorkee, Uttaranchal, India, 247661
        • Arogyam Institute ofParamedical and AlliedSciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age from 5 Years to 15 Years, Gender: Both, Details: Children who underwent abdominal surgery, having stable vitals, admitted in PICU and pediatric wards

Exclusion Criteria:

  • Patients with severe neurological illness, uncooperative patients, comatose patients, patients who are unwilling to enroll in study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Rehabilitation
Chest Physiotherapy including Percussion, vibration and shaking; along with it aerobic exercises such as walking up and down stairs, bedside ambulation, step walking

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Spirometey, manual muscle testing
Time Frame: 3 weeks
3 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 10, 2024

Primary Completion (Actual)

August 11, 2024

Study Completion (Actual)

August 11, 2024

Study Registration Dates

First Submitted

October 21, 2024

First Submitted That Met QC Criteria

October 21, 2024

First Posted (Actual)

October 22, 2024

Study Record Updates

Last Update Posted (Actual)

October 26, 2024

Last Update Submitted That Met QC Criteria

October 22, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REF20241002

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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