Chest Physiotherapy and Aerobic Training in Children Post Abdominal Surgery

NCT ID: NCT06653764

Last Updated: 2024-10-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

23 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-07-10

Study Completion Date

2024-08-11

Brief Summary

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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.

Detailed Description

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Conditions

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Post Abdominal Surgery

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Rehabilitation

Group Type EXPERIMENTAL

Chest physiotherapy and aerobic exercise training

Intervention Type OTHER

Chest Physiotherapy including Percussion, vibration and shaking; along with it aerobic exercises such as walking up and down stairs, bedside ambulation, step walking

Interventions

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Chest physiotherapy and aerobic exercise training

Chest Physiotherapy including Percussion, vibration and shaking; along with it aerobic exercises such as walking up and down stairs, bedside ambulation, step walking

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

5 Years

Maximum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Jazan

OTHER_GOV

Sponsor Role lead

Responsible Party

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Vandana Esht

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Arogyam Institute ofParamedical and AlliedSciences

Roorkee, Uttarakhand, India

Site Status

Countries

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India

Other Identifiers

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REF20241002

Identifier Type: -

Identifier Source: org_study_id

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