Faculty of Physical Therapy Cairo University
Giza, Dokki, 12612, Egypt
NCT Number: NCT07601568
To investigate the effect of PMI release on subacromial space, pectoralis minor length, shoulders ROM, shoulder joint pain, and functional ability in patients with SAIS.
This study is active but is not currently recruiting participants.
Notify Me40 year–60 year
All sexes
Interventional
Not applicable
Giza, Dokki, 12612, Egypt
Statement of the problem:
This study will be designed to answer the following question Does PMI release have an effect on subacromial space in patients with SAIS?
The purposes of the study:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
All patients who have any of the following will be excluded from the study (Lewis and Valentine 2007)
Physiotherapy treatment included passive manual joint mobilization, home-based strengthening exercises and advice on posture, twice a week.
So, we will apply this conventional physical therapy to control group
Treatment will be conventional treatment with pectoralis minor release and stretch.
Time frame: 6 months
The radiograph will be done to measure acromio-humeral distance, which is considered the shortest distance between the inferior cortex of acromion and the top of humeral head. In normal shoulders, the sub acromial space was between 9 and 10 mm. The space was significantly greater in men, with a slight reduction with age. In middle age, a sub-acromial space less than 6 mm is pathological
Time frame: 6 month
Participants will be asked to remain in a relaxed posture with the arms at the side in a neutral position, avoid postural correction, and exhale just before the measurement.
A tape measure was used to measure the linear distance between the origin and insertion of the muscle. The primary investigator of the study performed all measurements. The origin was defined as the inferior aspect of the 4th rib, which was one finger width lateral to the sternum, just lateral to the sternocostal junction. The insertion was defined as the medial-inferior aspect of the coracoid process .
Time frame: 6 month
Shoulder flexion, abduction, internal and external rotation movements will be measured with the individual seated upright on a non-reclining high-back chair, to limit trunk compensation. The chair was the same for all movements performed by one individual, but different for each individual, to provide support up to the middle of the scapula.
Shoulder movements will be actively and passively evaluated for flexion in supine and seated positions, abduction, external rotation in a neutral position with 0° abduction (ERN), external rotation with the arm at 90° of abduction (ER90), and internal rotation with the arm at 90° of abduction (IR90) using an Acumar digital inclinometer .
Time frame: 6 month
The patients' pain severity will be evaluated using a visual analog scale (VAS). The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between 0 "no pain" and 10 "worst pain
Time frame: 6 month
The disabilities of the arm, shoulder and hand (DASH) questionnaire is a self-administered region-specific outcome instrument developed as a measure of self-rated upper extremity disability and symptoms The use of the DASH questionnaire as an outcomes instrument in patients with upper-extremity complaints. The main part of the Quick-DASH is a 14-item disability/symptom scale concerning the patient's health status during the preceding week. The items ask about the degree of difficulty in performing different physical activities as well as the problem's impact on social activities, work, sleep, and self-image. Each item has five response options. The scores for all items are then used to calculate a scale score ranging from 1 (no difficulty) to 5 ( unable).
Cairo University
Other
Efficacy of Pectoralis Minor Release on Subacromial Space in Patients With Subacromial Impingement Syndrome
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07692516
Agnosia, Carpal Tunnel Syndrome
Lleida, Spain
View Trial DetailsNCT06778551
Behavior, Joint Diseases
Soria, Spain
View Trial DetailsNCT00637013
Joint Diseases, Musculoskeletal Diseases
Helsinki, Finland
View Trial DetailsNCT07675655
Joint Diseases, Musculoskeletal Diseases
Sohag, Tahta, Egypt
View Trial Details