Effect of Cervical Mobilization on Rotator Cuff Tendinitis

NCT04703660 | Unknown DMC

• 1 other identifier: interventional
• Study Type: interventional
• Target: 45
• Locations: 1 country
• Sites: 1

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

Conditions

Rotator Cuff Tendinitis

Outcome Measures

Primary Outcomes (3)

• 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

  before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization

• 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

  before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization

• change in pain level

  pain severity will be measured using visual analogue scale for 3 groups

  before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization

Study Arms (3)

group A

ACTIVE COMPARATOR

This group will receive antero-posterior cervical mobilization at c5-6 grade III oscillation

Procedure: cervical mobilization

group B

ACTIVE COMPARATOR

This group will receive lateral glide cervical mobilization at c5-6 grade III oscillation

Procedure: cervical mobilization

group C

ACTIVE COMPARATOR

This group will receive postero-anterior cervical mobilization at c5-6 grade III oscillation

Procedure: cervical mobilization

Interventions

cervical mobilization PROCEDURE

3 types of cervical mobilization at the level of C 5- 6

group A; group B; group C

Eligibility Criteria

• Age: 25 Years - 40 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• patients will be included if they have rotator cuff tendinitis

You may not qualify if:

• 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.

Sponsors & Collaborators

• Noha Elserty: lead

Study Sites (1)

Noha Elserty

Cairo, Egypt

RECRUITING

MeSH Terms

Conditions

Rotator Cuff Injuries

Condition Hierarchy (Ancestors)

Rupture; Wounds and Injuries; Shoulder Injuries; Tendon Injuries

Study Officials

• Noha S Elserty, PhD

  Lecturer of physical therapy- Egyptian Chinese University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Noha S Elserty, PhD

CONTACT

+201006709648; noha_elserty@hotmail.com

Rania R Mohamed, PhD

CONTACT

+201273325285; raniareda22@Hotmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: lecturer of physical therapy

Study Record Dates

• First Submitted: January 7, 2021
• First Posted: January 11, 2021
• Study Start: February 1, 2021
• Primary Completion: June 1, 2021
• Study Completion: June 1, 2021
• Last Updated: May 11, 2021

Record last verified: 2021-05

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, SAP
• Time Frame: after publishing the study

Locations

EG (1)