Back to resultsEffect of Cervical Mobilization on Rotator Cuff Tendinitis
Primary Purpose
Rotator Cuff Tendinitis
Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
cervical mobilization
Sponsored by
About this trial
This is an interventional treatment trial for Rotator Cuff Tendinitis
Eligibility Criteria
Inclusion Criteria:
- patients will be included if they have rotator cuff tendinitis
Exclusion Criteria:
- Patients will be excluded if they had recent neck trauma or acute whiplash disorder ,any intra articular injection in the gleno-humeral joint during last three months, patients with musculoskeletal disorder (any type of fracture), any history of surgery on that shoulder and tendon calcification, cervical rib, rotator cuff tear.
Sites / Locations
- Noha ElsertyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
group A
group B
group C
Arm Description
This group will receive antero-posterior cervical mobilization at c5-6 grade III oscillation
This group will receive lateral glide cervical mobilization at c5-6 grade III oscillation
This group will receive postero-anterior cervical mobilization at c5-6 grade III oscillation
Outcomes
Primary Outcome Measures
change in strength of shoulder abductors
strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder abductors
change in strength of shoulder external rotators
strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder external rotators
change in pain level
pain severity will be measured using visual analogue scale for 3 groups
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04703660
Brief Title
Effect of Cervical Mobilization on Rotator Cuff Tendinitis
Official Title
Immediate and Carry Over Effect of Different Cervical Mobilization Techniques on Rotator Cuff Tendinitis Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
June 1, 2021 (Anticipated)
Study Completion Date
June 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Noha Elserty
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
this study aimed to investigate the effect of 3 types of cervical mobilization on the strength of shoulder abductors, external rotators and pain level in patient with rotator cuff tendinitis. the measurement will be made immediately, 10 minutes, and 30 minutes after mobilization
Detailed Description
subjects will be allocated according to the inclusion and exclusion criteria from outpatient clinic at El sahel teaching hospital. they will be assigned randomly into 3 groups, each group will receive certain type of cervical mobilization. the outcome measures will be measured before, immediate, 10 minutes, and 30 minutes after treatment
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tendinitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
45 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
group A
Arm Type
Active Comparator
Arm Description
This group will receive antero-posterior cervical mobilization at c5-6 grade III oscillation
Arm Title
group B
Arm Type
Active Comparator
Arm Description
This group will receive lateral glide cervical mobilization at c5-6 grade III oscillation
Arm Title
group C
Arm Type
Active Comparator
Arm Description
This group will receive postero-anterior cervical mobilization at c5-6 grade III oscillation
Intervention Type
Procedure
Intervention Name(s)
cervical mobilization
Intervention Description
3 types of cervical mobilization at the level of C 5- 6
Primary Outcome Measure Information:
Title
change in strength of shoulder abductors
Description
strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder abductors
Time Frame
before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization
Title
change in strength of shoulder external rotators
Description
strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder external rotators
Time Frame
before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization
Title
change in pain level
Description
pain severity will be measured using visual analogue scale for 3 groups
Time Frame
before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients will be included if they have rotator cuff tendinitis
Exclusion Criteria:
Patients will be excluded if they had recent neck trauma or acute whiplash disorder ,any intra articular injection in the gleno-humeral joint during last three months, patients with musculoskeletal disorder (any type of fracture), any history of surgery on that shoulder and tendon calcification, cervical rib, rotator cuff tear.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Noha S Elserty, PhD
Phone
+201006709648
Email
noha_elserty@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rania R Mohamed, PhD
Phone
+201273325285
Email
raniareda22@Hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Noha S Elserty, PhD
Organizational Affiliation
Lecturer of physical therapy- Egyptian Chinese University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Noha Elserty
City
Cairo
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Noha S Elserty, PhD
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
supporting information that will be shared after publication of the study
IPD Sharing Time Frame
after publishing the study
Learn more about this trial
Effect of Cervical Mobilization on Rotator Cuff Tendinitis
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