None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age of participants 40 years to 65 years Participants of any gender Unilateral affection with loss of atleast 25 percent range of motion (active and passive) compared to non-involved shoulder in one or more directions Diagnosed and referred by orthopaedic surgeon. Participants who are willing to give written informed consent
Exclusion criteria
Exclusion criteria: Participants who are not able to complete the scales or Questionnaire Recent injury and fractures around the shoulder complex and cervical spine in the last 6 months Any surgeries around the shoulder joint and participants who received intra-articular injections in the last 6 months Psychiatric disorder Uncooperative participants Diagnosed with shoulder subluxation, dislocation, septic arthritis and rheumatoid arthritis Participants who are not willing to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS and SPADI scaleTimepoint: Visual analogue scale is used for assessing the intensity of pain pretreatment and post treatment at baseline and 6th week Shoulder Pain and Disability Index is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities used to assess at the baseline and at the 6th week Both the scales are assessed at baseline and 6th week | — |
Secondary
| Measure | Time frame |
|---|---|
| Shoulder range of motionTimepoint: Shoulder range of motion is measured through universal goniometer. Ranges measured are active & passive outcome measure is assessed at baseline & at 6th week | — |
Countries
India
Contacts
SDM College of Physiotherapy