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Effect of Cervical Mobilization on Rotator Cuff Tendinitis

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04703660
Recruitment Status : Recruiting
First Posted : January 11, 2021
Last Update Posted : May 11, 2021
Sponsor:
Information provided by (Responsible Party):
Noha Elserty, Egyptian Chinese University

Study Description
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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

Condition or disease Intervention/treatment Phase
Rotator Cuff Tendinitis Procedure: cervical mobilization Not Applicable

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
Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 45 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Immediate and Carry Over Effect of Different Cervical Mobilization Techniques on Rotator Cuff Tendinitis Patients
Actual Study Start Date : February 1, 2021
Estimated Primary Completion Date : June 1, 2021
Estimated Study Completion Date : June 1, 2021
Arms and Interventions
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Arm Intervention/treatment
Active Comparator: group A
This group will receive antero-posterior cervical mobilization at c5-6 grade III oscillation
 Procedure: cervical mobilization
3 types of cervical mobilization at the level of C 5- 6
Active Comparator: group B
This group will receive lateral glide cervical mobilization at c5-6 grade III oscillation
 Procedure: cervical mobilization
3 types of cervical mobilization at the level of C 5- 6
Active Comparator: group C
This group will receive postero-anterior cervical mobilization at c5-6 grade III oscillation
 Procedure: cervical mobilization
3 types of cervical mobilization at the level of C 5- 6


Outcome Measures
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Primary Outcome Measures :
  1. change in strength of shoulder abductors [ Time Frame: before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization ]
    strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder abductors

  2. change in strength of shoulder external rotators [ Time Frame: before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization ]
    strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder external rotators

  3. change in pain level [ Time Frame: before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization ]
    pain severity will be measured using visual analogue scale for 3 groups


Eligibility Criteria
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Ages Eligible for Study:   25 Years to 40 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
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.
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04703660


Contacts
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Contact: Noha S Elserty, PhD +201006709648 noha_elserty@hotmail.com
Contact: Rania R Mohamed, PhD +201273325285 raniareda22@Hotmail.com

Locations
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Egypt
Noha Elserty Recruiting
Cairo, Egypt
Contact: Noha S Elserty, PhD         
Sponsors and Collaborators
Noha Elserty
Investigators
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Principal Investigator: Noha S Elserty, PhD Lecturer of physical therapy- Egyptian Chinese University
More Information
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Responsible Party: Noha Elserty, lecturer of physical therapy, Egyptian Chinese University
ClinicalTrials.gov Identifier: NCT04703660    
Other Study ID Numbers: interventional
First Posted: January 11, 2021    Key Record Dates
Last Update Posted: May 11, 2021
Last Verified: May 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: supporting information that will be shared after publication of the study
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Time Frame: after publishing the study

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Tendinopathy
Rotator Cuff Injuries
Muscular Diseases
Musculoskeletal Diseases
 Tendon Injuries
Wounds and Injuries
Rupture
Shoulder Injuries