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Effect of Cervical Mobilization on Rotator Cuff Tendinitis

Immediate and Carry Over Effect of Different Cervical Mobilization Techniques on Rotator Cuff Tendinitis Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04703660
Enrollment
45
Registered
2021-01-11
Start date
2021-02-01
Completion date
2021-06-01
Last updated
2021-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator Cuff Tendinitis

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

Interventions

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

Sponsors

Noha Elserty
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
25 Years to 40 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
change in strength of shoulder abductorsbefore treatment, immediate, 10 minutes, and 30 minutes after cervical mobilizationstrength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder abductors
change in strength of shoulder external rotatorsbefore treatment, immediate, 10 minutes, and 30 minutes after cervical mobilizationstrength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder external rotators
change in pain levelbefore treatment, immediate, 10 minutes, and 30 minutes after cervical mobilizationpain severity will be measured using visual analogue scale for 3 groups

Countries

Egypt

Contacts

Primary ContactNoha S Elserty, PhD
noha_elserty@hotmail.com+201006709648
Backup ContactRania R Mohamed, PhD
raniareda22@Hotmail.com+201273325285

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026