An interventional study of cervical mobilization in Rotator Cuff Tendinitis, sponsored by Noha Elserty. Status unknown at 1 site in Egypt. Open to participants aged 25 Years to 40 Years. Per ClinicalTrials.gov, last updated 2021-05-11.
Sponsored by Noha Elserty · Not applicable, Interventional, and Treatment
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
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
413 studies on the registry are indexed under Tendinopathy; 64 are open to participants now.
This study's planned enrollment of 45 is close to the median of 50 across 339 interventional studies indexed under Tendinopathy.
Browse Tendinopathy studies →Noha Elserty is the lead sponsor of 2 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
This group will receive antero-posterior cervical mobilization at c5-6 grade III oscillation
Procedure: cervical mobilization
This group will receive lateral glide cervical mobilization at c5-6 grade III oscillation
Procedure: cervical mobilization
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
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
Time frame: 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
Time frame: 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
Time frame: before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization
Plan to share: Yes — supporting information that will be shared after publication of the study
Supporting information: Study protocol, Sap
No publications or documents are linked to this record.
This study is status unknown, as verified in May 2021. You cannot join it, but the record below documents what was studied.
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Noha Elserty