Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06019780
Other study ID # RiphahIU Hina Yasmeen
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date February 25, 2024

Study information

Verified date May 2024
Source Riphah International University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this research is to determine the effect of blood flow restriction training on shoulder pain, range of motion, muscle strength and shoulder. Randomized controlled trials will be done at Lady Reading Hospital Peshawar and Shahab Orthopedic General Hospital. The sample size is 36. The subjects will be divided in two groups, 18 subjects in BFR group and 18 in no BFR group. Study duration is 6 months. Sampling technique applied was non probability connivance sampling technique. Tools used in the study are SPADI shoulder score, NPRS, hand held dynamometer, sphygmomanometer and goniometer.


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.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date February 25, 2024
Est. primary completion date January 30, 2024
Accepts healthy volunteers No
Gender All
Age group 40 Years to 60 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
blood flow restriction trainin
Following exercise will be performed Side lying external rotation Prone horizontal abduction Standing scaption Individual in the group will be having two session per week, 16 session of exercise training for 8 weeks.50% of arterial occlusion pressure (60 to 80 mmHg) will be applied for total duration of 15mins. Occlusion pressure will be calculated according to formula for each patient [Pressure=0.4x(systolic BP)+2.7x(shoulder circumference)+62].4 sets with one set of 30 repetition and three sets of 15 repetition. After each set subject will have 30 seconds of rest with cuff inflated.
exercise
Following exercises will be performed without application of pneumatic cuff Side lying external rotation Prone horizontal abduction Standing scaption Conventional treatment will include: Hot pack 5 mins Maitland grade 3 and 4 mobilization: inferior glide (10reps x3sets), posterior glide (10reps x 3sets), anterior glide (10 reps x 3sets) Home plan: wand exercise, pendulum exercise, wall walking exercise (10reps x 2sets each)

Locations

Country Name City State
Pakistan Shahab orthopedic general hospital Peshawar KPK

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary shoulder apin the shoulder pain will be measured by NPRS, it has 11 points with 0 no pain and 10 extreme pain. baseline to 4th to 8 weeks
Primary Shoulder flexors strength 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
Primary Shoulder extensors strength 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
Primary Shoulder abductors strength this will be measured by the dynamometer by placing the dynamometer over the muscles and the individual will apply abduction force against isometric resistance. baseline to 8 weeks
Primary Shoulder rotation strength this will be measured by the dynamometer by placing the dynamometer over the muscles and the individual will apply rotation force against isometric resistance. baseline to 8 weeks
Primary Shoulder disability (SPADI) 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 shoulder flexion measures the shoulder flexion range of motion through goniometry baseline to 8 weeks
Secondary Shoulder extension measures the shoulder extension range of motion through goniometry baseline to 8 weeks
Secondary shoulder abduction measures the shoulder abduction range of motion through goniometry baseline to 8 weeks
Secondary shoulder adduction measures the shoulder adduction range of motion through goniometry baseline to 8 weeks
Secondary shoulder internal rotation measures the shoulder internal rotation range of motion through goniometry baseline to 8 weeks
Secondary shoulder external rotation measures the shoulder external rotation range of motion through goniometry baseline to 8 weeks
See also
  Status Clinical Trial Phase
Not yet recruiting NCT03245476 - Education-based Physical Therapy Approach for Adhesive Capsulitis N/A
Recruiting NCT03462420 - Physiotherapy Program for Managing Adhesive Capsulitis in Patients With Diabetes N/A
Recruiting NCT06181461 - Gong's Versus Kaltenborn Mobilization on Pain, Range of Motion and Function in Adhesive Capsulitis N/A
Completed NCT03678038 - Comparison of Rotator Interval Injection Versus Intraarticular Hydrodilatation in Frozen Shoulder N/A
Completed NCT01458691 - Intra-articular Injection of Allogeneic Platelet Rich Plasma (PRP) for Adhesive Capsulitis N/A
Recruiting NCT01449227 - Natural Course of Adhesive Capsulitis of Hip N/A
Terminated NCT00875862 - Shoulder Adhesive Capsulitis and Ambulatory Continuous Interscalene Nerve Blocks Phase 4
Completed NCT05402540 - Effectiveness of SCS Technique Verses ART in Adhesive Capsulitis N/A
Completed NCT05398588 - Spencer's Muscle Energy Technique and Cyriax Deep Friction Massage on Adhesive Capsulitis N/A
Recruiting NCT03676829 - Embolization for the Treatment of Pain Secondary to Adhesive Capsulitis Phase 1/Phase 2
Active, not recruiting NCT06404814 - Effectiveness of Functional Electrical Stimulation Versus Spencer Technique in Patients With Adhesive Capsulitis N/A
Completed NCT06062654 - Ultrasound-guided Hydrodistension in Patients With Adhesive Capsulitis N/A
Completed NCT05897866 - Sayed Issa's Hybrid Shoulder Arthroscopic-Open Surgical Management (HSSM) N/A
Completed NCT04822324 - Spencer's Muscle Energy Technique Along With Strain Counter Strain in Adhesive Capsulitis. N/A
Recruiting NCT06041282 - Conservative Treatment of Early Adhesive Capsulitis N/A
Withdrawn NCT03770546 - Amnion-Based Injections in the Shoulder N/A
Completed NCT06064396 - Effects of Gong's Mobilization With and Without Stecco Fascial Therapy in Patients With Adhesive Capsulitis N/A
Completed NCT04852939 - Bowen's Technique in Patients With Adhesive Capsulitis N/A
Completed NCT05655611 - Muscle Energy Technique With Or Without First Rib Mobilization In Adhesive Capsulitis N/A
Recruiting NCT04653636 - MRI and Clinical Predictive Factors of the Response to Arthrographic Distension in Severe Capsulitis