- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05039138
EFFECT OF NEUROMUSCULAR TRAINING ON SHOULDER FUNCTION
EFFECT OF NEUROMUSCULAR TRAINING ON SHOULDER FUNCTION IN PATIENTS WITH SHOULDER IMPINGEMENT SYNDROME: A DOUBLE BLINDED RANDOMIZED CONTROLLED TRIAL
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Double-blinded randomized controlled trial (patient and research assistant (the examiner of all patients) will be blinded).
Participants:
Thirty-four patients of both genders will be selected through non-probability sampling diagnosed as Neer's stage II SIS and their age range from 25-45 years will be randomly assigned to 1 of 2 groups. Each patient will sign an informed consent before starting the study (Appendix III).
Eligible patients will be recruited by physical therapist via referral from the treating orthopedic surgeon who will diagnose SIS based on clinical and radiological examination.
Group I (control): it includes 17 patients who will receive traditional strength training program.
Group II (experimental): it includes 17 patients who will receive upper extremity neuromuscular training exercises
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: aya ahmed nada, master degree
- Phone Number: +201285859034
- Email: elnour653@gmail.com
Study Contact Backup
- Name: maha mostafa mohammed, associate professor
- Phone Number: +201118803232
- Email: maha.mostafa@pt.cu.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patient age from 25-40 with a clinical diagnosis of Neer's stage II SIS (Consigliere et al., 2018).
Shoulder pain for at least three months (Heron et al., 2017) Painful arc of movement during flexion or abduction (Heron et al., 2017). Positive Neer's or Kennedy- Hawkins Test (Heron et al., 2017). Pain on resisted external rotation, abduction or Empty Can Test (Ager et al., 2019).
Exclusion Criteria:
Symptoms of cervical radiculopathy. Diagnosed inflammatory disorder. Neurological disorder. Widespread pain condition. Evidence of complete RC tear (positive drop arm test). Previous surgery to the affected shoulder.
:
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group I (control)
: it includes 17 patients who will receive traditional strength training program.
|
traditional strength training exercises in group I
|
Experimental: Group II (experimental):
it includes 17 patients who will receive upper extremity neuromuscular training exercises
|
patients will receive neuromuscular training exercises in group II
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
SPADI (The Shoulder Pain and Disability Index)
Time Frame: 6 weeks
|
It is a self-report questionnaire for shoulder function
|
6 weeks
|
Inclinometer
Time Frame: 6 weeks
|
joint position sense
|
6 weeks
|
Hand held dynamometer
Time Frame: 6 weeks
|
isometric muscle strength
|
6 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- shoulder neuromuscular
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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