Ignite Creation Date:
2024-05-06 @ 5:40 PM
Last Modification Date:
2024-10-26 @ 2:33 PM
Study NCT ID:
NCT05398549
Status:
COMPLETED
Last Update Posted:
2022-06-01
First Post:
2022-04-28
Brief Title:
Effects of Virtual Reality in Adhesive Capsulitis on Pain Range of Motion and Function
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Effects of Virtual Reality in Adhesive Capsulitis on Pain Range of Motion and Function
Status:
COMPLETED
Status Verified Date:
2022-05
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:
Adhesive capsulitis AC also known as frozen shoulder typically manifests to decrease range of motion ROM and function and increase pain in shoulder Objective of this study is to find the effects of virtual reality VR in adhesive capsulitis on pain range of motion and function to decrease pain and improve range of motion and function The study design will be a quasi-experimental study that will be used to compare the effects of virtual reality with conventional physical therapy Subjects with adhesive capsulitis meeting the predetermined inclusion amp exclusion criteria will be divided into two groups using lottery method Pre assessment will be done using visual analogue scale VAS shoulder pain and disability index SPADI tool and active shoulder flexion and abduction as subjective measurements Subjects in group A will be treated with virtual reality stimulation given for 30 minutes per session through kinetic Xbox with sensory accelerator model no1414 Two traditional training activities will be used to improve shoulder Range of motion ie shoulders finger ladder training activity and single curved shoulder training activity 12 times 3 rounds in each practice of the training 1 Patients will be required to complete standard training task by interacting with designed VR rehabilitative training games under the supervision of physical therapists and subjects in group B will be treated with conventional physical therapy ie grade 1 and 2 mobilization and stretching exercise Baseline treatment protocol hot pack will be applied to both groups
Treatment duration for both groups will be 30 minutes Each subject will receive a total 6 week protocol with 02 treatment sessions per week Post treatment reading will be recorded after the end of 2 nd 4th and 6th treatment weeks Recorded values will be analyzed for any change using SPSS 21
Treatment duration for both groups will be 30 minutes Each subject will receive a total 6 week protocol with 02 treatment sessions per week Post treatment reading will be recorded after the end of 2 nd 4th and 6th treatment weeks Recorded values will be analyzed for any change using SPSS 21
Detailed Description:
None
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?:
None
Is an FDA AA801 Violation?:
None