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Night Pain in Patients With Rotator Cuff Syndrome

Primary Purpose

Shoulder Pain, Shoulder Impingement Syndrome, Shoulder Tendinitis

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Night Pain in Patients with Rotator Cuff Syndrome
Sponsored by
Gaziosmanpasa Research and Education Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Shoulder Pain focused on measuring Pain, Shoulder, Rotator Cuff

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • To be diagnosed with rototor cuff pathology by magnetic resonance imaging
  • Age range between 18-65 years old
  • To be literate and cooperative

Exclusion Criteria:

  • Having shoulder pathology other than rototor cuff pathology (Glenohumeral instability, Bisipital tendon lesions, Glenohumeral joint osteoarthritis, Acromioclavicular joint osteoarthritis, Milwaukee shoulder)
  • Having complete rotator cuff tear
  • Patients with a history of shoulder or cervical surgery
  • The presence of cervical pathology
  • Patients with a history of fracture in the shoulder with pain
  • Local corticosteroid injection history for the shoulder (over the last 6 months) and using painkiller regularly
  • Physical therapy history for the shoulder (in the last 3 months)
  • The presence of systemic inflammatory disease
  • Malignancy
  • Pregnancy
  • A history of any psychiatric disorders

Sites / Locations

  • Alper Mengi

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Patients with Rotator Cuff Syndrome

Arm Description

The patients diagnosed with rotator cuff syndrome by clinical and magnetic resonance imaging.

Outcomes

Primary Outcome Measures

Night pain: visual analogue scale
The pain severity was evaluated using a 10 cm visual analogue scale , where 0 represented no pain, while 10 represented unbearable pain.At evaluation, the average of the pain during night for the last one week were inquired.

Secondary Outcome Measures

Demographic datas
Gender, Age, Education Level, Job
Daytime pain: visual analogue scale
The pain severity was evaluated using a 10 cm visual analogue scale , where 0 represented no pain, while 10 represented unbearable pain.At evaluation, the average of the pain during daytime for the last one week were inquired.
Range of Motion of the Shoulder
The shoulder range of motion of the patients will be measured in the form of active range of motion and using a goniometer. The shoulder range of motion will be measured as flexion, extension, internal rotation, external rotation, abduction and adduction.
Pathology in magnetic resonance imaging
The rotator cuff pathologies will be evaluated in MR imaging as subacromial-subdeltoid effusion, supraspinatus muscle tendinosis, supraspinatus muscle tear, supraspinatus muscle calcific tendinitis, infraspinatus muscle tendinosis, infraspinatus muscle tear, teres minör muscle tendinosis, teres minör muscle tear, subscapularis muscle tendinosis, subscapularis muscle tear.
The Shoulder Pain and Disability Index
The Shoulder Pain and Disability Index (SPDA) is a self-administered questionnaire that consists of two dimensions (for pain and for functional activities). The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper-extremity use. Each of the 13 items is to be rated with a number from 0 to 10: For the pain score (first 5 items): 0 means no pain and 10 means worst pain imaginable; For the disability score (last 8 items): 0 means no impairment and 10 means the patient requires help to perform that action. Scores could theoretically range from 0 to 100 with higher scores indicating greater impairment. The total SPADI score was calculated by averaging the pain and disability subscale scores. The total SPADI score could also range from 0 to 100.
Tampa Scale of Kinesiophobia
Tampa Scale of Kinesiophobia is a 17-item self report checklist using a 4-point Likert scale that was developed as a measure of fear of movement or (re)injury. The TSK is a self-completed questionnaire and the range of scores are from 17 to 68 where the higher scores indicate an increasing degree of kinesiophobia.
The Short Form-36
Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
Body mass index
The formula is Body mass index = kg/m2 where kg is a person's weight in kilograms and m2 is their height in metres squared.
pain duration
The duration of pain will be asked to patients as months.
history of trauma to the shoulder
It will be questioned whether patients had a history of trauma to the shoulder before.
dominant hand and affected arm side
The patients will be asked which hands are dominant (right or left), and the side with shoulder pain (right or lelft) will be recorded.
smoking history
Patients will be asked about their smoking habit for the last 6 months.
diabetes history
The patients will be asked whether they have diabetes disease.
Hawkins test
Hawkins test is performed by elevating the patient's arm forward to 90 degrees while forcibly internally rotating the shoulder. Patients will be evaluated for positive test or negative test.
Neer test
Neer test is performed by placing the arm in forced flexion with the arm fully pronated . The scapula is stabilized during the maneuver to prevent scapulothoracic motion. Patients will be evaluated for positive test or negative test.
Painful arc test
The patient fully abducts their arm in the scapular plane , and is considered positive if the patient reports pain between 60 degrees and 120 degrees of abduction.
Jobe test
The patient's arm elevates to 90 degrees in the scapular plane, with the elbow extended, full internal rotation, and pronation of the forearm. This results in a thumbs-down position, as if the patient were pouring liquid out of a can, and the patient tries to resist this motion. This test is considered positive if the patient experiences pain or weakness with resistance.
drop-arm test
This test is performed by passively abducting the patient's shoulder, then observing as the patient slowly lowers the arm to the waist. Patients will be evaluated for positive test or negative test.
Patte test
The examiner places the patient's arm to 90 degrees in the scapular plane and flexes the elbow to 90 degrees . The patient is then asked to externally rotate against resistance. The test is positive if the patient is unable to perform external rotation.
External rotation test
The examiner passively flexes the patient's elbow to 90 degrees and brings the shoulder into a position of 20 degrees of scaption. Next, the examiner passively takes the patient's shoulder into a position of maximal lateral rotation. The patient in then instructed to hold that position. A positive test is if the patient cannot maintain the position and the shoulder rotates internally.
Lag sign test
The elbow is passively flexed to 90° and the shoulder abducted to 90° and held 5° off maximal external rotation. The patient is then asked to maintain the position actively while the examiner releases the wrist while maintaining support through the elbow.Patients will be evaluated for positive test or negative test.
Gerber lift-off test
The patient is examined in standing and is asked to place their hand behind their back with the dorsum of the hand resting in the region of the mid- lumbar spine. The dorsum of the hand is raised off the back by maintaining or increasing internal rotation of the humerus and extension at the shoulder. Inability to move the dorsum off the back constitutes an abnormal lift-off test and indicates subscapularis rupture or dysfunction.

Full Information

First Posted
March 21, 2019
Last Updated
May 12, 2020
Sponsor
Gaziosmanpasa Research and Education Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03894761
Brief Title
Night Pain in Patients With Rotator Cuff Syndrome
Official Title
What Are the Factors Affecting Night Pain in Patients With Rotator Cuff Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
March 21, 2019 (Actual)
Primary Completion Date
December 30, 2019 (Actual)
Study Completion Date
December 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Gaziosmanpasa Research and Education Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to determine the factors that may be associated with night pain in patients diagnosed with rotator cuff syndrome by clinical and magnetic resonance imaging.
Detailed Description
Patients who were diagnosed as rotator cuff syndrome by clinical examination and magnetic resonance imaging will be included in this prospective study. Demographic data (gender, age, education level, occupation), shoulder pain duration, history of trauma to the shoulder, smoking, dominant arm and diabetes will be questioned and body mass indexes will be calculated. Active shoulder range of motion of the patients will be measured by goniometer and recorded . Specific tests, which are important for rotator cuff lesion, will be performed to determine whether they are positive or not. Magnetic resonance imaging of the patients with shoulder pathology will be recorded. A visual analog scale will be used to determine the intensity of day and night pain. Shoulder Shoulder Pain and Disability Index to assess shoulder disability of patients, SF-36 form will be filled by patient to evaluate the effect of shoulder pathology and Kinesiophobia Score to assess the avoidance of pain induced movement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Shoulder Pain, Shoulder Impingement Syndrome, Shoulder Tendinitis, Rotator Cuff Tear
Keywords
Pain, Shoulder, Rotator Cuff

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
61 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients with Rotator Cuff Syndrome
Arm Type
Other
Arm Description
The patients diagnosed with rotator cuff syndrome by clinical and magnetic resonance imaging.
Intervention Type
Other
Intervention Name(s)
Night Pain in Patients with Rotator Cuff Syndrome
Intervention Description
The pain severity was evaluated using a 10 cm visual analogue scale , where 0 represented no pain, while 10 represented unbearable pain.At evaluation, the average of the pain during night for the last one week were inquired.
Primary Outcome Measure Information:
Title
Night pain: visual analogue scale
Description
The pain severity was evaluated using a 10 cm visual analogue scale , where 0 represented no pain, while 10 represented unbearable pain.At evaluation, the average of the pain during night for the last one week were inquired.
Time Frame
7 day
Secondary Outcome Measure Information:
Title
Demographic datas
Description
Gender, Age, Education Level, Job
Time Frame
1 day
Title
Daytime pain: visual analogue scale
Description
The pain severity was evaluated using a 10 cm visual analogue scale , where 0 represented no pain, while 10 represented unbearable pain.At evaluation, the average of the pain during daytime for the last one week were inquired.
Time Frame
7 day
Title
Range of Motion of the Shoulder
Description
The shoulder range of motion of the patients will be measured in the form of active range of motion and using a goniometer. The shoulder range of motion will be measured as flexion, extension, internal rotation, external rotation, abduction and adduction.
Time Frame
1 day
Title
Pathology in magnetic resonance imaging
Description
The rotator cuff pathologies will be evaluated in MR imaging as subacromial-subdeltoid effusion, supraspinatus muscle tendinosis, supraspinatus muscle tear, supraspinatus muscle calcific tendinitis, infraspinatus muscle tendinosis, infraspinatus muscle tear, teres minör muscle tendinosis, teres minör muscle tear, subscapularis muscle tendinosis, subscapularis muscle tear.
Time Frame
1 day
Title
The Shoulder Pain and Disability Index
Description
The Shoulder Pain and Disability Index (SPDA) is a self-administered questionnaire that consists of two dimensions (for pain and for functional activities). The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper-extremity use. Each of the 13 items is to be rated with a number from 0 to 10: For the pain score (first 5 items): 0 means no pain and 10 means worst pain imaginable; For the disability score (last 8 items): 0 means no impairment and 10 means the patient requires help to perform that action. Scores could theoretically range from 0 to 100 with higher scores indicating greater impairment. The total SPADI score was calculated by averaging the pain and disability subscale scores. The total SPADI score could also range from 0 to 100.
Time Frame
7 days
Title
Tampa Scale of Kinesiophobia
Description
Tampa Scale of Kinesiophobia is a 17-item self report checklist using a 4-point Likert scale that was developed as a measure of fear of movement or (re)injury. The TSK is a self-completed questionnaire and the range of scores are from 17 to 68 where the higher scores indicate an increasing degree of kinesiophobia.
Time Frame
7 days
Title
The Short Form-36
Description
Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.
Time Frame
7 days
Title
Body mass index
Description
The formula is Body mass index = kg/m2 where kg is a person's weight in kilograms and m2 is their height in metres squared.
Time Frame
1 day
Title
pain duration
Description
The duration of pain will be asked to patients as months.
Time Frame
1 day
Title
history of trauma to the shoulder
Description
It will be questioned whether patients had a history of trauma to the shoulder before.
Time Frame
1 day
Title
dominant hand and affected arm side
Description
The patients will be asked which hands are dominant (right or left), and the side with shoulder pain (right or lelft) will be recorded.
Time Frame
1 day
Title
smoking history
Description
Patients will be asked about their smoking habit for the last 6 months.
Time Frame
6 months
Title
diabetes history
Description
The patients will be asked whether they have diabetes disease.
Time Frame
1 day
Title
Hawkins test
Description
Hawkins test is performed by elevating the patient's arm forward to 90 degrees while forcibly internally rotating the shoulder. Patients will be evaluated for positive test or negative test.
Time Frame
1 day
Title
Neer test
Description
Neer test is performed by placing the arm in forced flexion with the arm fully pronated . The scapula is stabilized during the maneuver to prevent scapulothoracic motion. Patients will be evaluated for positive test or negative test.
Time Frame
1 day
Title
Painful arc test
Description
The patient fully abducts their arm in the scapular plane , and is considered positive if the patient reports pain between 60 degrees and 120 degrees of abduction.
Time Frame
1 day
Title
Jobe test
Description
The patient's arm elevates to 90 degrees in the scapular plane, with the elbow extended, full internal rotation, and pronation of the forearm. This results in a thumbs-down position, as if the patient were pouring liquid out of a can, and the patient tries to resist this motion. This test is considered positive if the patient experiences pain or weakness with resistance.
Time Frame
1 day
Title
drop-arm test
Description
This test is performed by passively abducting the patient's shoulder, then observing as the patient slowly lowers the arm to the waist. Patients will be evaluated for positive test or negative test.
Time Frame
1 day
Title
Patte test
Description
The examiner places the patient's arm to 90 degrees in the scapular plane and flexes the elbow to 90 degrees . The patient is then asked to externally rotate against resistance. The test is positive if the patient is unable to perform external rotation.
Time Frame
1 day
Title
External rotation test
Description
The examiner passively flexes the patient's elbow to 90 degrees and brings the shoulder into a position of 20 degrees of scaption. Next, the examiner passively takes the patient's shoulder into a position of maximal lateral rotation. The patient in then instructed to hold that position. A positive test is if the patient cannot maintain the position and the shoulder rotates internally.
Time Frame
1 day
Title
Lag sign test
Description
The elbow is passively flexed to 90° and the shoulder abducted to 90° and held 5° off maximal external rotation. The patient is then asked to maintain the position actively while the examiner releases the wrist while maintaining support through the elbow.Patients will be evaluated for positive test or negative test.
Time Frame
1 day
Title
Gerber lift-off test
Description
The patient is examined in standing and is asked to place their hand behind their back with the dorsum of the hand resting in the region of the mid- lumbar spine. The dorsum of the hand is raised off the back by maintaining or increasing internal rotation of the humerus and extension at the shoulder. Inability to move the dorsum off the back constitutes an abnormal lift-off test and indicates subscapularis rupture or dysfunction.
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: To be diagnosed with rototor cuff pathology by magnetic resonance imaging Age range between 18-65 years old To be literate and cooperative Exclusion Criteria: Having shoulder pathology other than rototor cuff pathology (Glenohumeral instability, Bisipital tendon lesions, Glenohumeral joint osteoarthritis, Acromioclavicular joint osteoarthritis, Milwaukee shoulder) Having complete rotator cuff tear Patients with a history of shoulder or cervical surgery The presence of cervical pathology Patients with a history of fracture in the shoulder with pain Local corticosteroid injection history for the shoulder (over the last 6 months) and using painkiller regularly Physical therapy history for the shoulder (in the last 3 months) The presence of systemic inflammatory disease Malignancy Pregnancy A history of any psychiatric disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alper Mengi, M.D.
Organizational Affiliation
Gaziosmanpasa Research and Education Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alper Mengi
City
Çanakkale
ZIP/Postal Code
17100
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No

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Night Pain in Patients With Rotator Cuff Syndrome

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