Title of This Study is to Evaluate the Effects of Abdominal Drawing in Maneuver With Cross Pattern Limb Exercises in Patients With Subacromial Impingement Syndrome

April 7, 2026 updated by: Ishrat Fatima, Superior University

Effects of Abdominal Drawing-In Maneuver With Cross-Pattern Limb Exercises on Pain, Disability, and Range of Motion in Shoulder Impingement Syndrome.

SUMMARY :

Introduction: Shoulder impingement syndrome is a slowly progressive disease.Among people with shoulder pain, shoulder impingement syndrome (SIS) has the highest prevalence and accounts for 36% of shoulder disorders.Most studies have examined the effect of stretching and strengthening exercises on the glenohumeral joint (shoulder joint).

Objective:The objective of this study is to determine the effect of the Abdominal Drawing-In Maneuver combined with Cross-Pattern Limb Exercises on pain and disability and range of motion in patients with Shoulder Impingement Syndrome.

Methodology: This study will be Randomized Controlled Trial and 38 subjects will be taken for the study those who fulfills the inclusion criteria. They will be randomly divided into two groups, in control group only conventional treatment and in experimental trial group, conventional treatment as well as abdominal drawing in maneuver with cross pattern limb exercises will be given. Each subject of the study will be treated for a period of 4 weeks, 3 days a week, one session per day. An assessment will be done prior to starting of treatment, after 4 weeks of treatment, again assessment will be taken for these subjects. Pain and disability is measured by using NPRS, SPADI and range of motion flexion, abduction, external rotation and internal rotation will be measured by using Goniometer. The data will be analyzed using SPSS version 25, quantitative variables will be presented using mean, standard deviation, range, histograms. Categorical variables will be presented as frequencies, percentages, cross tabulation and bar charts, pie charts. Normality of data will be analyzed by shapiro-wilk test. Parametric independent t-test will be used to check difference between the groups and paired t-test will be used to find difference within the group.

Study Overview

Study Type

Interventional

Enrollment (Actual)

38

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

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 53720
        • Suyperior Univeristy

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:

  1. Patients with age group 30-50
  2. Both male and females
  3. Positive Neer's sign, positive Hawkins Kennedy sign, ,
  4. Pain with positive painful arc. Pain with resisted isometric abduction

Exclusion Criteria:

  1. History of shoulder dislocation
  2. Patients underwent any shoulder joint surgery.
  3. Fracture of upper limb.
  4. Patient who has current symptoms related to the cervical spine,
  5. Patient who has a history of acromioclavicular pain
  6. Patient having history low back pain 7Corticosteroid injection into the shoulder joint in the previous 12 months

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group with abdominal Drawing in maneuvour with cross pattern limb exercises

Heating pad will be applied over the shoulder area for about 15 minutes at the start of each session. The intervention plan will be given as follows:

  1. Abdominal drawing-in with alternating upper extremity movement, (The patient will lie in supine position and draw his abdomen downwards and will move his alternate upper extremity upwards.
  2. Abdominal drawing-in with alternating lower extremity movement, (The patient will lie in supine position and draw his abdomen downwards and will move his alternate lower extremity upward and downwards
  3. Abdominal drawing-in with alternating upper and lower extremity movement, (The patient will lie in supine position and draw his abdomen downwards and move alternate upper and lower extremity upward and downwards.
  4. Opposite arm leg raises in prone position
  5. Bridge exercise
  6. Wall climbing,
  7. Wand exercises,
  8. Shoulder ROMS,
  9. Prone arm elevation,
  10. Cross-Chest Stretch
  11. Pendulum Exercises
  1. Abdominal drawing-in with alternating upper extremity movement,
  2. Abdominal drawing-in with alternating lower extremity movement,
  3. Abdominal drawing-in with alternating upper and lower extremity movement,
  4. Opposite arm leg raises in prone position,
  5. Bridge exercise
Active Comparator: Conventional Study group

Half of the particpants will be treated with only shoulder conventional exercises. Heating pad will be applied over the shoulder area for about 15 minutes at the start of each session.

Following exercises will be performed in control group:

  1. Wall climbing,
  2. Wand exercises,
  3. Shoulder ROMS,
  4. Prone arm elevation,
  5. Cross-Chest Stretch Pendulum Exercises
The participants in conventional group will only receive shoulder exercises that will include Wall climbing, Wand exercises, Shoulder ROMS, Prone arm elevation, Cross-Chest Stretch Pendulum Exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
NPRS
Time Frame: The pain assessment is done pre treatment on day 1 week 1 before 1st session and second assessment is done on 12th sesion after 4 weeks
It is numeric pain rating scale ranging from 0-10. Patient will rate his pain from 0-10 with 0 means no pain and 10 with severe pain.
The pain assessment is done pre treatment on day 1 week 1 before 1st session and second assessment is done on 12th sesion after 4 weeks
Shoulder Pain and Disability Index
Time Frame: The assessment is taken pre treatment day 1 week 1 before 1st session and second assessment is taken on 12th session after 4 weeks
SPADI scale consists of 5 questions with 10 points each related to pain and 8 question related to disability with 10 points each totalling 140 points.
The assessment is taken pre treatment day 1 week 1 before 1st session and second assessment is taken on 12th session after 4 weeks
Goniometry
Time Frame: Range of motion is assessed pre treatment on day 1 week 1 before 1st session and 2nd assessment is taken on 12th session after 4 weeks.
Goniometry is used to assess range of motion. Goniometer is used to measure it. Flexion, abduction, internal and external rotations are measured using goniometer.
Range of motion is assessed pre treatment on day 1 week 1 before 1st session and 2nd assessment is taken on 12th session after 4 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)

February 20, 2026

Primary Completion (Estimated)

April 20, 2026

Study Completion (Estimated)

April 20, 2026

Study Registration Dates

First Submitted

March 24, 2026

First Submitted That Met QC Criteria

April 7, 2026

First Posted (Actual)

April 13, 2026

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 7, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

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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