Effects of Thrower's Ten and Routine Physical Therapy in Patients With Shoulder Impingement Syndrome
1 other identifier
interventional
46
1 country
1
Brief Summary
To compare the effects of thrower's ten and routine physical therapy on pain, range of motion and functional disability in patients with shoulder impingement syndrome
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 2024
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 1, 2024
CompletedFirst Submitted
Initial submission to the registry
May 6, 2024
CompletedFirst Posted
Study publicly available on registry
May 9, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 10, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 10, 2024
CompletedMay 9, 2024
May 1, 2024
8 months
May 6, 2024
May 6, 2024
Conditions
Outcome Measures
Primary Outcomes (3)
Numeric Pain Rating Scale
The Numeric Pain Rating Scale (NPRS) is used to assess pain. On an 11-point Numeric scale, 0 represents the least amount of pain (no pain) and 10 Represents the most amount of pain (worst pain)
6 weeks
Range of Motion
It is frequently employed as a benchmark technique for the assessment of Range of Motion (ROM) as the main component of all joint motions. The range of mobility of a joint is measured using a device known as a goniometer. Goniometry is the art and science of measuring the joint ranges in every plane of the joint. Short arm and long arm versions of the universal goniometer are available. Goniometric measurements are highly reliable provided measurements are conducted by the same therapist. Shoulder Abduction, Flexion and External rotation range will be taken by a Universal Goniometer.
6 weeks
Shoulder pain and disability index (SPADI)
The SPADI (Shoulder Pain and impairment Index) was created to assess current shoulder pain and impairment in an outpatient environment. The SPADI consists of 13 items that assess two domains: a 5-item subscale for pain and an 8-item subscale for disability. The SPADI has since been used in both primary care on mixed diagnosis and surgical patient populations including rotator cuff disease, osteoarthritis, and rheumatoid arthritis, adhesive capsulitis ,joint replacement surgery , and in a large population-based study of shoulder symptoms
6 weeks
Study Arms (2)
Thrower's Ten Exercise Program
EXPERIMENTAL1. D2 PNF flexion 2. D2 PNF extension 3. Internal rotation 4. External rotation 5. Push ups 6. Press ups
Routine physical therapy
SHAM COMPARATOR1. Unilateral bench press 2. Bi lateral shoulder retraction 3. Extension in prone position 4. Neck retraction. Then isometrics will be performed which includes 1\. Isometric shoulder internal and external rotation 2. Side lying shoulder external rotation 3. Scapular scaption exercise
Interventions
No Of Sessions Per Week: 3 Per Weeks for 6 weeks (50 Min per Session) No of repetitions; 2 sets for 10 repetitions with 1 minute rest between sets.
In this, the exercises will be performed in 2 sets and 10 repetitions with 5-10s hold and 30s to 1min rest between repetitions. No Of Sessions Per Week: 3 Per Weeks for 6 weeks (50 Min Per Session)
Eligibility Criteria
You may qualify if:
- Age group 18-35 years
- Male and female
- Shoulder or neck pain within the prior 6month
- positive tests out of 5: Positive Neer's test, positive Hawkins test, positive Jobe's test, painful arc, and pain on resisted external rotation of the arm.
You may not qualify if:
- History of surgery of the affected shoulder
- Fractures in around the shoulder
- Neurological disorders leading to altered muscle activity
- Systemic arthritic conditions (RA, Osteoporosis)
- Disorders of the cervical spine
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Johar Pain Relief Center
Lahore, Punjab Province, 54782, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rabiya Noor, PHD
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 6, 2024
First Posted
May 9, 2024
Study Start
February 1, 2024
Primary Completion
October 10, 2024
Study Completion
November 10, 2024
Last Updated
May 9, 2024
Record last verified: 2024-05
Data Sharing
- IPD Sharing
- Will not share