- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05973695
Effects of Clamshell Versus Gluteal Bridge Exercises
Effects of Clamshell Versus Gluteal Bridge Exercises on Low Back Pain, Gluteal Strength and Disability Due to Prolonged Sitting in Females With Gluteal Amnesia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Jinnah Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Female between the ages of 20 to 40 years
- Prolonged sitting hours >4 hours.
- Examination- Symptoms provoked by low back movement.
- Positive Gluteal strength test
- Positive SLR for hamstring tightness
- Positive Thomas test for Rectus femoris tightness.
Exclusion Criteria:
• Osteoporosis
- Malignancy
- Vertebral fractures
- Pervious or scheduled surgery
- Trauma
- Pregnancy
- Psychological conditions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group A: Clamshell Exercise
Group A will be treated with baseline treatment and clamshell exercises.
Lie on your side with your knees slightly bent and with one leg on top of the other.
Keep your feet together and lift your top knee until its parallel with your hip.
Lower your knee back to the initial position, repeat, and then switch sides.
In 1st week 1 sets 10 repetitions.
In 2nd week 2 sets of 10 repetitions.
In 3rd and 4th week and onwards 3 sets of 10 repetitions.
|
For clamshell exercises, Lie on your side with your knees slightly bent and with one leg on top of the other.
Keep your feet together and lift your top knee until its parallel with your hip.
Lower your knee back to the initial position, repeat, and then switch sides.
In 1st week 1 sets 10 repetitions.
In 2nd week 2 sets of 10 repetitions.
In 3rd and 4th week and onwards 3 sets of 10 repetitions
|
|
Active Comparator: Group B: Gluteal Bridge exercise
Group B will be treated with baseline treatment and Gluteal Bridge exercises.
Start flat on your back with your legs bent at a 90-degree angle and feet placed flat on the ground.
Make sure your toes are turned outward at 45-degree angles and your knees are facing in the same direction as your toes.
Drive down through your feet and push your hips up.
You should feel this variation fatiguing the outer portion of your thighs.
Make sure you keep your knees over your toes throughout the entire movement.
Don't let them move forward over the toes.
In a controlled motion, let your hips sink back down toward the ground.
This completes 1 repetition.
Perform 3 sets of 15 repetitions, or 3 rounds of a 30-second hold.
|
Start flat on your back with your legs bent at a 90-degree angle and feet placed flat on the ground.
Make sure your toes are turned outward at 45-degree angles and your knees are facing in the same direction as your toes.
Drive d
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numerical Pain Rating scale (NPRS)
Time Frame: upto 4 weeks
|
The numerical Pain Rating scale (NPRS) assesses the pain in the gluteal region. Pain is assessed using a Numeric pain rating (NPRS). The scale ranges from 0 to 10. 0 indicates "no pain", and 10 indicates "worst Pain. mild pain score 1 to 3 moderate pain score 4 to 7 severe pain score with interference with functioning. 8 to 10 |
upto 4 weeks
|
|
Oswestry disability score
Time Frame: upto 4 weeks
|
Oswestry Disability score is used to measure low back disability. Each ten item is scored from 0 to 5, and the total is added and multiplied by 2. Therefore, the ODI ranges from 0 to 100. A higher score on the ODI indicates a more severe disability caused by LBP. Oswestry Disability Index will evaluate disability for disability. This questionnaire will be used to assess disability. It comprises 10 items, 7 related to daily activities, 2 related to pain, and 1 related to concentration. Each item scores from 0 to 5. The total score is expressed as a percentage with higher scores related to more significant disability |
upto 4 weeks
|
|
Quality of Life EQ-5D
Time Frame: upto 4 weeks
|
EQ-5D Health-Related Quality of Life Question checked the quality of life of the patients. Descriptive system for health-related quality of life states in adults, consisting of five dimensions (Mobility, Self-care, Usual activities, Pain & discomfort, Anxiety & depression), each with five severity levels described by statements appropriate to that dimension. The scale ranges from 100 ('the best imaginable health state' or 'the best health state you can imagine') to 0 ('the worst imaginable health state' or 'the worst health you can imagine'). This is used to obtain a respondent's stated preference values, not to record their own health state. |
upto 4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Samrood Akram, Mphil, Riphah International University,Lahore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- REC/RCR & AHS/23/0128 UMIA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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