Trunk Extensor Endurance Training Versus Scapular Mobilization in Patient With Thoracic Kyphosis

June 25, 2024 updated by: Shamaila Yaqub, Riphah International University

Comparison of Trunk Extensor Endurance Training Versus Scapular Mobilization in Patient With Thoracic Kyphosis.

To compare the effect of Trunk extensor endurance training and scapular mobilization on thoracic pain in patient with thoracic kyphosis.

To compare the effect of Trunk extensor endurance training and scapular mobilization on kyphotic angle in patient with thoracic kyphosis To compare the effect of Trunk extensor endurance training and scapular mobilization on shoulder ROM in patient with thoracic kyphosis

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

28

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 Contact

Study Locations

  • Pakistan
    • Khyber Pakhutunkhuwa
      • Peshawar, Khyber Pakhutunkhuwa, Pakistan, 25000
        • Recruiting
        • Lady Reading Hospital(LRH)
        • Contact:
        • Principal Investigator:
          • Uzma Akbar, MS-OMPT
        • Sub-Investigator:
          • Shamaila Yaqub

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

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Both gender (Male and female)
  • Age 20-40
  • Postural kyphosis
  • Kyphotic angle exceeds 40°
  • Thoracic pain>3

Exclusion Criteria:

  • Thoracic, Scapular and clavicle abnormalities
  • Vertebral fractures, history of trauma or spinal surgery
  • History of prolonged use steroid (more than 6 months),rheumatologic conditions
  • Cardiac, autoimmune diseases
  • Structural kyphosis(X-ray findings)
  • Scoliosis(x-ray findings)
  • Cancer, neurological disorders, metastasis, or inflammatory
  • Osteoporosis, Pregnancy or any genetic conditions affecting their bones, muscles or cartilage.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 1(Trunk Extensor Endurance Training)
Trunk Extensor Endurance Training Level 1: Prone shoulder extension or prone shoulder raises Level 2: Prone back extension Level 3: Prone Ys or Y raises Level 4:Superman pose Level 5:Superman or prone cobra (The given position should be hold for 10 seconds and performs 25 repetitions with 3 sec rests in between the efforts)
Other: Trunk Extensor Endurance training & Scapular mobilization

Trunk Extensor Endurance Training Level 1:Prone shoulder extension or prone shoulder raises Level 2: Prone back extension Level 3: Prone Ys or Y raises Level 4:Super man pose Level 5:Super man or prone cobra

(The given position should be hold for 10 seconds and performs 25 repetitions with 3 sec rests in between the efforts)

Scapular Mobilization:

Intervention program includes, supero-inferior, medio-lateral along with circumduction movements).

3 sets of 10-15 repetitions of each of the supero-inferior ,medio-lateral, and circumduction movements Between each session, there was a10 or 30-second break. The length of rests was adjusted depending on the patient's endurance
Experimental: Group 2(Scapular Mobilization)

Patient side lying. This intervention program includes, supero-inferior, medio-lateral along with circumduction movements.

Procedure:

Patients were side lying with their arms in 90°flexion during scapula mobilization.

The physiotherapist completed 3 sets of 10-15 repetitions of each of the supero-inferior, medio-lateral, and circumduction movements while holding the scapula from the medial border. Between each session, there was a 10 or 30-second break. The length of rests was adjusted depending on the patient's endurance and comfort.
Other: Trunk Extensor Endurance training & Scapular mobilization

Trunk Extensor Endurance Training Level 1:Prone shoulder extension or prone shoulder raises Level 2: Prone back extension Level 3: Prone Ys or Y raises Level 4:Super man pose Level 5:Super man or prone cobra

(The given position should be hold for 10 seconds and performs 25 repetitions with 3 sec rests in between the efforts)

Scapular Mobilization:

Intervention program includes, supero-inferior, medio-lateral along with circumduction movements).

3 sets of 10-15 repetitions of each of the supero-inferior ,medio-lateral, and circumduction movements Between each session, there was a10 or 30-second break. The length of rests was adjusted depending on the patient's endurance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Thoracic pain
Time Frame: 4 weeks
NPRS(Numeric pain rating scale)
4 weeks
kyphotic angle
Time Frame: 4 weeks
Inclinometer
4 weeks
Shoulder ROM
Time Frame: 4 weeks
Goniometer
4 weeks

Collaborators and Investigators

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

Sponsor

Riphah International University

Investigators

  • Principal Investigator: Shamaila Yaqub, masters, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Estimated)

June 1, 2024

Primary Completion (Estimated)

June 26, 2024

Study Completion (Estimated)

July 7, 2024

Study Registration Dates

First Submitted

June 25, 2024

First Submitted That Met QC Criteria

June 25, 2024

First Posted (Estimated)

July 1, 2024

Study Record Updates

Last Update Posted (Estimated)

July 1, 2024

Last Update Submitted That Met QC Criteria

June 25, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/MS-PT/01678

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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