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
Effects of Abdominal Drawing-In Maneuver With Cross-Pattern Limb Exercises on Pain, Disability, and Range of Motion in Shoulder Impingement Syndrome.
1 other identifier
interventional
38
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 20, 2026
CompletedFirst Submitted
Initial submission to the registry
March 24, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 20, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 20, 2026
CompletedApril 13, 2026
March 1, 2026
2 months
March 24, 2026
April 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
NPRS
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
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
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.
Study Arms (2)
Experimental group with abdominal Drawing in maneuvour with cross pattern limb exercises
EXPERIMENTALHeating 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
Conventional Study group
ACTIVE COMPARATORHalf 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
Interventions
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
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
Eligibility Criteria
You may qualify if:
- Patients with age group 30-50
- Both male and females
- Positive Neer's sign, positive Hawkins Kennedy sign, ,
- Pain with positive painful arc. Pain with resisted isometric abduction
You may not qualify if:
- History of shoulder dislocation
- Patients underwent any shoulder joint surgery.
- Fracture of upper limb.
- Patient who has current symptoms related to the cervical spine,
- Patient who has a history of acromioclavicular pain
- Patient having history low back pain 7Corticosteroid injection into the shoulder joint in the previous 12 months
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Suyperior Univeristy
Lahore, Punjab Province, 53720, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr. Ishrat Fatima PT
Study Record Dates
First Submitted
March 24, 2026
First Posted
April 13, 2026
Study Start
February 20, 2026
Primary Completion
April 20, 2026
Study Completion
April 20, 2026
Last Updated
April 13, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share