- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06019780
Effects of Blood Flow Restriction Training in Patients With Adhesive Capsulitis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Frozen shoulder is painful shoulder condition associated with stiffness and shoulder disability. It is associated with reduction in forward elevation and marked external rotation. Frozen shoulder is common condition effecting population between ages 30 to 60 years. Prevalence is more common in women than on men There are four stages of adhesive capsulitis, stage1, stage 2 (freezing stage), stage 3 (frozen stage) and stage 4 (thawing stage). Patient have sharp pain at end range of motion, sleep disturbances and early loss of external rotation. When compared to asymptomatic subjects, patients with adhesive capsulitis have higher upper trapezius to lower trapezius EMG ratios during arm elevation, indicating a muscular imbalance. The scapula eventually migrates upward before 60 degrees of abduction in individuals with adhesive capsulitis, resulting in the recognizable "shrug sign" during shoulder elevation.
Blood flow is restricted in a controlled form of vascular occlusion using external tourniquet. A recent study demonstrated that augmentation of low load resistance with blood flow restriction (L-L BFR) to contractile tissue can produce hypertrophy and strength gains, using loads as low as 30% 1RM. BFR exercise may stimulate skeletal muscle growth and strength gains through a number of different methods. These could include an increase in hormone levels, an increase in the motor pathway or other intracellular signaling pathways for muscle protein synthesis, an increase in satellite cell activity biomarkers, and apparent patterns in fibre type recruitment.
The purpose of this study is to provide the effects of blood flow restriction training on shoulder discomfort, range of motion, muscle strength and disability in patients with adhesive capsulitis. Due to pain and decrease range of motion individual with adhesive capsulitis experience muscle weakness in shoulder joint. Blood flow restriction training has positive effect on improvement of muscle strength and range of motion in shoulder region. Blood flow restriction training has also positive effect on bone healing and bone density. Therefore the study is aimed to improve the muscles strength and capsule inflammation in individual with adhesive capsulitis.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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KPK
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Peshawar, KPK, Pakistan, 46000
- Shahab orthopedic general hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Frozen shoulder (stage 2 and 3 of Kisner and Colby's classification system)
- Male and female
- Patients whose age lies between 40 and 60
- Ranges restriction in forward flexion (scaption) less than 100 degree and reduction of external and internal rotation to less than 50% of the normal
Exclusion Criteria:
• History of Cardiovascular diseases
- DVT patients
- Hypertensive patients
- Patients having neurological disease
- Fracture of humerus
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: Experimental interventional group A (Blood flow restriction training)
Following exercise will be performed
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Following exercise will be performed
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Active Comparator: Control group B
Following exercise will be performed
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Following exercises will be performed without application of pneumatic cuff
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
shoulder apin
Time Frame: baseline to 4th to 8 weeks
|
the shoulder pain will be measured by NPRS, it has 11 points with 0 no pain and 10 extreme pain.
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baseline to 4th to 8 weeks
|
|
Shoulder flexors strength
Time Frame: baseline to 8 weeks
|
this will be measured by the dynamometer by placing the dynamometer over the muscles and the individual will apply flexion force against isometric resistance.
|
baseline to 8 weeks
|
|
Shoulder extensors strength
Time Frame: baseline to 8 weeks
|
this will be measured by the dynamometer by placing the dynamometer over the muscles and the individual will apply extension force against isometric resistance.
|
baseline to 8 weeks
|
|
Shoulder abductors strength
Time Frame: baseline to 8 weeks
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this will be measured by the dynamometer by placing the dynamometer over the muscles and the individual will apply abduction force against isometric resistance.
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baseline to 8 weeks
|
|
Shoulder rotation strength
Time Frame: baseline to 8 weeks
|
this will be measured by the dynamometer by placing the dynamometer over the muscles and the individual will apply rotation force against isometric resistance.
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baseline to 8 weeks
|
|
Shoulder disability (SPADI)
Time Frame: baseline to 8 weeks
|
measure current shoulder pain and disability in an outpatient setting.
The SPADI contains 13 items that assess two domains; a 5-item subscale that measures pain and an 8-item subscale that measures disability.
|
baseline to 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
shoulder flexion
Time Frame: baseline to 8 weeks
|
measures the shoulder flexion range of motion through goniometry
|
baseline to 8 weeks
|
|
Shoulder extension
Time Frame: baseline to 8 weeks
|
measures the shoulder extension range of motion through goniometry
|
baseline to 8 weeks
|
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shoulder abduction
Time Frame: baseline to 8 weeks
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measures the shoulder abduction range of motion through goniometry
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baseline to 8 weeks
|
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shoulder adduction
Time Frame: baseline to 8 weeks
|
measures the shoulder adduction range of motion through goniometry
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baseline to 8 weeks
|
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shoulder internal rotation
Time Frame: baseline to 8 weeks
|
measures the shoulder internal rotation range of motion through goniometry
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baseline to 8 weeks
|
|
shoulder external rotation
Time Frame: baseline to 8 weeks
|
measures the shoulder external rotation range of motion through goniometry
|
baseline to 8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aisha Razzaq, MSPT-OMPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- RiphahIU Hina Yasmeen
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.
Clinical Trials on Adhesive Capsulitis
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Daniel G. RendeiroCompletedAdhesive Capsulitis of Shoulder | Frozen Shoulder | Shoulder Adhesive CapsulitisUnited States
-
University of MalayaNot yet recruitingAdhesive Capsulitis of Shoulder
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Taipei Veterans General Hospital, TaiwanRecruitingAdhesive Capsulitis of ShoulderTaiwan
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Taif UniversityCompletedAdhesive Capsulitis of ShoulderSaudi Arabia
-
Riphah International UniversityCompletedAdhesive Capsulitis of ShoulderPakistan
-
Balikesir UniversityCompletedAdhesive Capsulitis of Shoulder
-
Haytham M ElhafezCairo UniversitySuspendedAdhesive Capsulitis of the ShoulderEgypt
-
Superior UniversityActive, not recruitingAdhesive Capsulitis, ShoulderPakistan
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