Ignite Creation Date:
2024-06-16 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06460675
Status:
RECRUITING
Last Update Posted:
2024-06-14
First Post:
2024-06-11
Brief Title:
Comparasion of Autogenic Inhibition and Reciprocal Inhibition Muscle Energy Techniques METS in Piriformis Syndrome
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Comparative Effects of Autogenic Inhibition and Reciprocal Inhibition Muscle Energy Techniques in Piriformis Syndrome
Status:
RECRUITING
Status Verified Date:
2024-06
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 Autogenic Inhibition and Reciprocal Inhibition Muscle Energy Techniques METS in Piriformis Syndrome
Detailed Description:
Piriformis syndrome is when the piriformis muscle located in the buttock region spasms and causes buttock pain The piriformis muscle also can irritate the nearby sciatic nerve and cause pain numbness and tingling along the back of the leg and into the foot similar to sciatic pain The functional limitations experienced by hip pain patients in the lower limb profoundly impact their quality of life This study aims to investigate the effectiveness of an integrated approach that compares the Effects of Autogenic Inhibition versus Reciprocal Inhibition Muscle Energy Techniques on Pain Range of motion and Disability in patients with Piriformis Syndrome
This randomized clinical trial will be conducted at DHQ Hospital Jhang over six months The sample size will consist of 32 participants Participants who meet the inclusion criteria will be taken through a non-probability convenience sampling technique that will be randomized through a sealed envelope method 16 Participants will be assigned to Group A that will be treated with the Autogenic Inhibition Muscle Energy Technique 16 Participants will be assigned to Group B and will be treated with Reciprocal Inhibition Muscle Energy Technique at the frequency of 1 set and 3 repetitions per session for two sessions per week and total six sessions for three weeks with follow up at one month The duration of contraction is 7-10 seconds Pre and post-intervention values will be taken on the 1st day in the 3rd week and at one-month follow-up Data will be collected using various assessment tools including the FAIR test Freiberg test Lasegue test Beatty test Pace sign Numeric Pain Rating Scale NPRS and Universal Goniometer Pre-intervention assessments will be conducted for all two groups The effects of the interventions will be measured either by parametric or non-parametric tests after assessing the normality of data by the Shapiro-Wilk test Independent t-test Data analysis will be performed by using SPSS 25 software
This randomized clinical trial will be conducted at DHQ Hospital Jhang over six months The sample size will consist of 32 participants Participants who meet the inclusion criteria will be taken through a non-probability convenience sampling technique that will be randomized through a sealed envelope method 16 Participants will be assigned to Group A that will be treated with the Autogenic Inhibition Muscle Energy Technique 16 Participants will be assigned to Group B and will be treated with Reciprocal Inhibition Muscle Energy Technique at the frequency of 1 set and 3 repetitions per session for two sessions per week and total six sessions for three weeks with follow up at one month The duration of contraction is 7-10 seconds Pre and post-intervention values will be taken on the 1st day in the 3rd week and at one-month follow-up Data will be collected using various assessment tools including the FAIR test Freiberg test Lasegue test Beatty test Pace sign Numeric Pain Rating Scale NPRS and Universal Goniometer Pre-intervention assessments will be conducted for all two groups The effects of the interventions will be measured either by parametric or non-parametric tests after assessing the normality of data by the Shapiro-Wilk test Independent t-test Data analysis will be performed by using SPSS 25 software
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