Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06535750
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-07-23
Brief Title:
Comparison Of The Effects Of Conventional Physiotherapy And Strengthening Exercises With Rotator Cuff Syndrome
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison Of The Effects Of Conventional Physiotherapy And Strengthening Exercises Additional To Conventional Physiotherapy On Pain Muscle Strength Joint Range Of Motion Functionality And Quality Of Life In Patients With Rotator Cuff Syndrome
Status:
COMPLETED
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Various options are available for the treatment of rotator cuff syndrome including conservative and surgical Conservative treatment methods include activity modification nonsteroidal anti-inflammatory drugs NSAIDs corticosteroid injections CSIs and physiotherapy Physiotherapy methods include various interventions such as manual therapy exercise and electrotherapy Although these treatments do not directly treat the specific pathology they help correct rotator cuff and scapular muscle weakness and dysfunction reduce the tightness of the posterior capsule and other soft tissues and relieve pain and dysfunction It focuses on correcting the postural abnormalities that contribute to the disease
In our study the investigators aimed to determine the effects of rehabilitation components in the conservative treatment of patients with rotator cuff syndrome and to determine the effects of strengthening exercises on the functional status of the patients
In our study the investigators aimed to determine the effects of rehabilitation components in the conservative treatment of patients with rotator cuff syndrome and to determine the effects of strengthening exercises on the functional status of the patients
Detailed Description:
Rotator cuff syndrome RCS also known as rotator cuff tendonitis is characterised by intense pain functional impairment loss of shoulder range of motion ROM nocturnal pain and limitations in activities of daily living It is a common problem in the ageing population and its patophysiology may be the result of tendon degeneration resulting from microtrauma repetitive activities overload or traumatic injury
Groups Participants were randomly divided into two treatment groups There are 10 patients in each group The patients in the control group received a standard treatment programme while the patients in the experimental group received strengthening exercises with theraband in addition to the standard treatment programme Treatment sessions for both groups lasted 50-55 minutes and were performed three days a week Details of the study groups are given below
Control Group
Patients in the control group received a standard treatment programme This programme included the following
Passive stretching exercises were performed 10 repetitions for each movement shoulder flexion abduction adduction internal rotation external rotation Codman exercises were performed 15 repetitions with 1kg dumbbell Shoulder isometric exercises were performed 15 repetitions for each movement ball press clockwise and anti-clockwise ball rotation finger slide on the wall Wand exercises were performed 15 repetitions shoulder abduction internal rotation external rotation Electrotherapy was applied for 20 minutes and ice therapy was applied for 20 minutes7-9 Experimental Group
Patients in the experimental group received strengthening exercises with theraband in addition to the standard treatment programme This programme included the following
Strengthening Exercises Low-row biceps strengthening shoulder horizontal abduction and shoulder horizontal adduction external rotation After the pain decreased strengthening exercises for subscapularis infraspinatus supraspinatus teres minor deltoid and scapulothoracic muscles were performed The colour of the Theraband was chosen between yellow red green blue and red to the extent tolerated by the patient
Groups Participants were randomly divided into two treatment groups There are 10 patients in each group The patients in the control group received a standard treatment programme while the patients in the experimental group received strengthening exercises with theraband in addition to the standard treatment programme Treatment sessions for both groups lasted 50-55 minutes and were performed three days a week Details of the study groups are given below
Control Group
Patients in the control group received a standard treatment programme This programme included the following
Passive stretching exercises were performed 10 repetitions for each movement shoulder flexion abduction adduction internal rotation external rotation Codman exercises were performed 15 repetitions with 1kg dumbbell Shoulder isometric exercises were performed 15 repetitions for each movement ball press clockwise and anti-clockwise ball rotation finger slide on the wall Wand exercises were performed 15 repetitions shoulder abduction internal rotation external rotation Electrotherapy was applied for 20 minutes and ice therapy was applied for 20 minutes7-9 Experimental Group
Patients in the experimental group received strengthening exercises with theraband in addition to the standard treatment programme This programme included the following
Strengthening Exercises Low-row biceps strengthening shoulder horizontal abduction and shoulder horizontal adduction external rotation After the pain decreased strengthening exercises for subscapularis infraspinatus supraspinatus teres minor deltoid and scapulothoracic muscles were performed The colour of the Theraband was chosen between yellow red green blue and red to the extent tolerated by the patient
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None