Ignite Creation Date:
2024-05-11 @ 8:31 AM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06407817
Status:
RECRUITING
Last Update Posted:
2024-05-09
First Post:
2024-05-06
Brief Title:
Comparative Effects Of Spencer and Reverse Distraction Technique In Patients With Adhesive Capsulitis
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Comparative Effects Of Spencer and Reverse Distraction Technique In Patients With Adhesive Capsulitis
Status:
RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To compare the effects of spencer and reverse distraction technique in patients with adhesive capsulitis
Detailed Description:
Adhesive capsulitis also known as frozen shoulder is an inflammatory condition characterized by shoulder stiffness pain and significant loss of passive range of motion Adhesive capsulitis has a prevalence of approximately 2 to 5 in the general population with a mean onset of age of 55
A randomized clinical trial will be conducted at Ibne Sina Hospital Multan Non probability convenience sampling technique will be applied on 50 patients who will be allocated through computerized randomization into group A group B to collect data Group A will be given spencer technique and group B will be given reverse distraction technique along with baselines The study will be completed within the time duration of ten months Primary Outcome measures of the research will be pain range of motion function muscle strength disability and quality of life will be measured pre and post intervention The whole treatment protocols will be given for four weeks Data will be analyzed using SPSS software version 25 After assessing normality of data by Shapiro-wilk test it will be decided either parametric or non-parametric test will be used within a group or between two groups
A randomized clinical trial will be conducted at Ibne Sina Hospital Multan Non probability convenience sampling technique will be applied on 50 patients who will be allocated through computerized randomization into group A group B to collect data Group A will be given spencer technique and group B will be given reverse distraction technique along with baselines The study will be completed within the time duration of ten months Primary Outcome measures of the research will be pain range of motion function muscle strength disability and quality of life will be measured pre and post intervention The whole treatment protocols will be given for four weeks Data will be analyzed using SPSS software version 25 After assessing normality of data by Shapiro-wilk test it will be decided either parametric or non-parametric test will be used within a group or between two groups
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None