Health TrialsbyHealthPanel

Effect of Shoulder Symptom Modification Procedure (SSMP) in Managing Patients with Frozen Shoulder

ConditionFrozen Shoulder
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-65
SponsorGulf Medical University

About this trial

the study is about intervention to patient with frozen shoulder to help patients improve function and shoulder disability , reduce pain and improve range of motion, the main aim of this study is to find out which treatment intervention SSMP , MWM and sham mobilization give effective results

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

• Diagnosis of adhesive capsulitis confirmed by a healthcare professional.

Scores more than 2 in adhesive capsulitis scale

Range of motion affected in capsular pattern

Age between 40-65 years.

Disqualifiers

Having any history of shoulder dislocation

Humerus fractures or trauma

Diagnosed with any sort of cancer

History of cardiovascular disease

Trial design

Design model

Parallel

Treatments tested in this trial

  • SSMP, Isometric exercise, eccentric exercise, heavy slow resistance , functional program

    Procedure/Surgery

    In this group the patients will be given symptom modification procedure in the first phase followed by isometric exercises in second phase, eccentrics and HSR in third phase and functional program in fourth phase

  • MWM,Isometric exercise, eccentric exercise, heavy slow resistance , functional program

    Procedure/Surgery

    in this mobilization with movement in first phase will be given followed by isometrics, eccentrics and heavy slow resistance exercise and finally the functional program

  • sham mobilization

    Procedure/Surgery

    Sham mobilization followed by isometrics, eccentric training and heavy resistance training and finally the functional program .

Treatment groups

36 Participants
are divided into 3 treatment groups
Group A: SSMPExperimental treatment 1 intervention
Group B: MWMExperimental treatment 1 intervention
Group C: sham mobilizationPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Shoulder Pain And Disability Index

shoulder pain and disability index is use to measure shoulder pain and disability where 0 is the best score and 130 is the worst

Time frame
from enrollment to week 4,6,8
2

Numeric Pain Rating Scale

numeric pain rating scale where 0 indicates no pain and 10 indicates worst pain

Time frame
from enrollment to 8 weeks

Secondary outcomes

1

Range Of Motion

range of motion of shoulder joint that includes flexion, extension abduction, adduction, internal and external rotation

Time frame
week 4,6,8
2

Patients' Global Impression of Change (PGIC) scale

PGIC is a 7 point scale depicting a patient's rating of overall improvement. where 1 indicates very much improved and 7 indicates worst

Time frame
at enrollment and on 8th week

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Gulf Medical University

Lead sponsor

Source ClinicalTrials.gov
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