- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06172192
EFFECTS OF CORE STRENGTHENING WITH RESISTIVE VERSUS NON-RESISTIVE DIAPHRAGMATIC TRAINING ON CORE ENDURANCE IN LOWER CROSS SYNDROME
Study Overview
Status
Conditions
Detailed Description
The purpose of this study is to determine the effects of core strengthening on trunk endurance after core strengthening with resistive versus non-resistive diaphragmatic training in lower cross syndrome.
Core stability of young adults (age: 19-30 years) will be determined using McGill's muscular endurance test battery:
- Flexor endurance test
- Extensor endurance test
- Right lateral endurance test
- Left lateral endurance test Scores will be taken three times for each test; the average of each text will be noted for each participant.
Data collection procedure: Participants of interest would be approached and explained about the research. Informed written consent will be taken. Recruited participants will be allocated to either of the groups through a sealed opaque envelope method. McGill's Torso Muscular Endurance Test Battery will be used and baseline and post-intervention scores will be recorded.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Fatima Aiman, MS-MSKPT*
- Phone Number: 0323-5495943
- Email: fatima.aiman966@gmail.com
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Recruiting
- Foundation University College of Physical Therapy
-
Contact:
- Qurat ul ain Saeed, MS-OMPT
- Phone Number: 03315562889
- Email: quratulain.saeed@fui.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 19-30 years
- Both genders
- Positive modified Thomas test
- Positive prone hip extension strength test
- Positive trunk flexion strength test
- Tight erector spinae
- Asia pacific BMI normal and overweight (18.5-24.9 Kg/m2)
- Local intermittent lumbar pain
- Mild to moderate pain (NPRS 1-6)
- Painless movement and activity
- Pain only produced by sustained loading in relevant position, which is then relieved on moving from that posture
Exclusion Criteria:
- Shoulder pain
- Acute flare LBP
- Centralization and peripheralization of pain (21)
- Intermittent pain at limited end range (21)
- Leg symptoms when walking, eased in flexion (Signs of stenosis) (21)
- Pain due to repetitive movement (21)
- Paresthesia/numbness (21)
- Structural deformity (Kyphosis, lordosis, scoliosis, spondylosis, spondylolysis, spondylolisthesis)
- Curve reversal (21)
- Pregnancy
- Post surgery
- Degenerative and inflammatory spinal diseases
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group A
Group A will perform Core Strengthening exercises. In addition to core strengthening protocol, non-resistive Diaphragmatic training group will perform self-diaphragm breathing exercises Core strengthening protocol will comprise of following three phases:
After performance of Core Strengthening protocol, Group A will perform Self-Diaphragmatic breathing exercises. |
After performance of core strengthening protocol, group A will perform self-diaphragmatic breathing exercises while group B will perform resistive diaphragmatic breathing exercise. Participants will place one hand on the chest and other on the abdomen, feeling the swelling of the stomach and the movement of the chest. It will be performed in supine position. Supervised breathing exercises in two sets for 15 minutes with 5 minutes break between sets and 10 minutes rest after it will be performed |
|
Experimental: Group B
Group B will perform Core Strengthening exercises. In addition to core strengthening protocol, resistive Diaphragmatic training group will perform resisted-diaphragm breathing exercises. Core strengthening protocol will comprise of following three phases:
After performance of Core Strengthening protocol, group B will perform Resistive Diaphragmatic Exercises. |
After performance of core strengthening protocol, group A will perform self-diaphragmatic breathing exercises while group B will perform resistive diaphragmatic breathing exercise. Participants will place one hand on the chest and another on the sand bag placed over abdomen. This sand bag weighing 3-5 Kgs will provide resistance to breathing. These exercises will be performed in supine position. We will adjust the weight of the sandbag as per individual's level of 11-13 of 'Rating of Perceived Exercise (RPE)'. Supervised breathing exercises in two sets for 15 minutes with 5 minutes break between sets and 10 minutes rest after it will be performed |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in trunk flexor endurance test
Time Frame: 6 weeks
|
Subject will sit on the test bench and place the upper body against a support with an angle of 60 ° from the test bed.
The arms will be folded across the chest with the hands placed on the opposite shoulder.
Subjects will be instructed to maintain the body position while the supporting wedge will be pulled back 10 cm to begin the test.
The test will end when the upper body fell below the 60 ° angle.
|
6 weeks
|
|
Change in trunk extensor endurance test
Time Frame: 6 weeks
|
Subjects will be laid prone with the lower body fixed to the test bed at the ankles, knees, and hips and the upper body extended.
Subjects will rest their upper bodies on the floor before the exertion.
At the beginning of the exertion, the upper limbs will be held across the chest with the hands resting on the opposite shoulders, and the upper body will be lifted off the floor until the upper torso is horizontal to the floor.
Subjects will be instructed to maintain the horizontal position as long as possible.
|
6 weeks
|
|
Left lateral endurance test
Time Frame: 6 weeks
|
The participants will assume a side-lying position with their legs fully extended and feet aligned on top of each other.
Upon readiness, they will be instructed to transition into a full side-bridge position, ensuring that both legs remain extended and the sides of the feet are in contact with the floor.
Timing will commence as they successfully maintain this position.
The test will conclude if there is any noticeable change in the alignment of the participant's trunk.
This test will be conducted twice with a 2-minute rest between intervals.
The average duration of the two tests will be recorded on the participant's record sheet.
The test will then
|
6 weeks
|
|
Right lateral endurance test
Time Frame: 6 weeks
|
The participants will assume a side-lying position with their legs fully extended and feet aligned on top of each other.
Their lower arm will be positioned under their body while the upper arm rests at their side.
Upon readiness, they will be instructed to transition into a full side-bridge position, ensuring that both legs remain extended and the sides of the feet are in contact with the floor.
Timing will commence as they successfully maintain this position.
The test will conclude if there is any noticeable change in the alignment of the participant's trunk.
This test will be conducted twice with a 2-minute rest between intervals.
The average duration of the two tests will be recorded on the participant's record sheet.
The test will then
|
6 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUI/CTR/2023/23
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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