Effects of Core Stability Exercises on Motor Control in Patients With Low Back Pain.
1 other identifier
interventional
44
1 country
1
Brief Summary
The aim of this research is aims to evaluate the effectiveness of core stability exercise on motor control, pain and disability in patients with low back pain. Randomized controlled trials will be done at Rehman Medical Institute. The sample size was 44. The subjects were divided in two groups, 22 subjects were given conventional therapy and 22 were given conventional therapy along with core stability exercises. Study duration was of 6 months. Sampling technique applied was non probability convenience sampling technique. Patient with age 30-50 years both Male \& female gender Presence of back pain for ≥6 weeks, MCI (Motor Control Impairment) complaints (pain provocation in static posture) with 3 or more positive tests were included. Tools used in the study are NPRS, ODI, and MCI tests.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable low-back-pain
Started Sep 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2024
CompletedFirst Submitted
Initial submission to the registry
November 12, 2024
CompletedFirst Posted
Study publicly available on registry
November 13, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 16, 2025
CompletedApril 18, 2025
April 1, 2025
7 months
November 12, 2024
April 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
MCI tests
First test is Waiters Bow test which includes flexion of hip 50-70⁰ in upright standing without movement (flexion) of low back. The second test is dorsal pelvic tilt in upright standing keeping thoracic spine neutral and lumbar spine moves towards flexion. The third tests involves normal standing to single leg stance and measurement of lateral movement of belly. Fourth test is upright sitting with knee extension. In this position lumbar spine should be neutral. Fifth test is quadruped position with pelvis moving back and fro i.e. rocking with low back in neutral. Hip should be flex 90-120⁰. The last test is prone lying with active knee flexion up to 90⁰ without movement of low back and pelvis. If 3 out 6 tests are positive then subject will be categorized as impaired motor control.
baseline to 6 weeks
Secondary Outcomes (2)
NPRS
baseline to 6 weeks
Oswestry Disability Index (ODI
baseline to 6 weeks
Study Arms (2)
Core stability Group A
EXPERIMENTALthe core stability group includes core stability exercises along with the general back, pelvis and piriformis stretches
Traditional therapy group B
ACTIVE COMPARATORthe traditional group includes general back, pelvis and piriformis stretches
Interventions
Abdominal hollowing in supine (10 reps \& 2 sets) Single leg bridge (10 reps \& 2 sets), 3 session per week for 6 weeks Prone Single leg raise(10 reps \& 2 sets) Double leg bridge (10 reps \& 2 sets) Abdominal hallowing in 4 point kneeling(10 reps \& 2 sets), Complete Back stretch Pelvic rotations Posterior Pelvic tilt Knee to chest Piriformis stretch Maitland mobilization ( based on assessment) 10 reps 10 sec hold 2 session per day
Complete Back stretch Pelvic rotations, 3 sessions per week for 6 week Posterior Pelvic tilt Knee to chest Piriformis stretch Maitland mobilization ( based on assessment) 10 reps 10 sec hold 2 session per day
Eligibility Criteria
You may qualify if:
- Both gender Presence of back pain for ≥6 weeks
- Age 30 -50 years
- MCI (Motor Control Impairment) complaints (pain provocation in static posture)
- Participants had 3 or more positive test out of six MCI tests.
You may not qualify if:
- LBP of specific cause, Recent spine surgery (\<6 weeks)
- Comorbid health condition(Spondylolesthesis, fracture, Spondylolysis)
- Constant pain below knee
- Patient who denied consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Rehman Medical Institute
Peshawar, Khybar Pakhtunkha, 25000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Aisha Razzaq, PHD*
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 12, 2024
First Posted
November 13, 2024
Study Start
September 1, 2024
Primary Completion
March 30, 2025
Study Completion
April 16, 2025
Last Updated
April 18, 2025
Record last verified: 2025-04
Data Sharing
- IPD Sharing
- Will not share