Compare The Effect of Pendulum Exercises With the Kaltenborn Mobilization Among the Patients of Adhesive Capsulitis
1 other identifier
interventional
38
1 country
1
Brief Summary
To determine the effect of pendulum exercises with the kaltenborn mobilization among the patients of adhesive capsulitis
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 18, 2023
CompletedStudy Start
First participant enrolled
April 1, 2023
CompletedFirst Posted
Study publicly available on registry
May 11, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2023
CompletedMay 11, 2023
May 1, 2023
2 months
March 18, 2023
May 10, 2023
Conditions
Outcome Measures
Primary Outcomes (2)
Shoulder Pain assessed by Visual Analog Scale
6 Months
disability index
6 Months
Study Arms (2)
Pendulum Exercises
OTHERKaltenborn Mobilization
EXPERIMENTALInterventions
Compare The Effect of Pendulum Exercises Among the Patients of Adhesive Capsulitis
Compare The Effect of Kaltenborn Mobilization Among the Patients of Adhesive Capsulitis
Eligibility Criteria
You may qualify if:
- Subjects will be of the age group of 40-60 years.
- Can be male or female
- Diagnosed with adhesive capsulitis by orthopedic or physical therapist.
- Pain, stiffness, and limitation of passive shoulder lateral rotation, abduction, and internal rotation of more than 50% compared with the opposite side for at least 3 months
You may not qualify if:
- Presence of neurological disorders (e.g., stroke, Parkinson's disease) leading to deficiency of shoulder muscles activity, Severe trauma related to painful stiff shoulder which leads to bony changes of the affected shoulder on radiographs, Previous surgeries and manipulation under anesthesia of the affected shoulder
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Superior University CRC
Lahore, Punjab Province, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 18, 2023
First Posted
May 11, 2023
Study Start
April 1, 2023
Primary Completion
June 1, 2023
Study Completion
August 31, 2023
Last Updated
May 11, 2023
Record last verified: 2023-05
Data Sharing
- IPD Sharing
- Will not share