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Low Back PainNCT06756685

Effects of Core Strengthening Versus Motor Control Training on Pain, Disability & Endurance in Low Back Pain

A study testing Core Strengthening Exercises in people with Low Back Pain, run by Riphah International University at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study aims to compare the effects of core strengthening versus motor control training on pain, disability \& endurance in patients with low back pain Read more about this study

Who is it for?
Ages 25 to 60 years
Conditions the study is for
Low Back Pain
What is being tested?
Core Strengthening Exercises
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
74 participants
Where
1 sitePakistan
Study dates
7 Aug 2024to 10 Jan 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Non-specific Chronic low back pain (>3 months)
  • Pain between the T12 vertebra and gluteal fold with pain of 2-8 on the numerical rating scale of 0-10
  • Both Genders
  • Age of 25 and above

Who cannot join

  • Participants fall in this category would be excluded of the study.
  • Lumbar radiculopathy
  • Structural scoliosis
  • Traumatic spinal injury
  • Cauda equina syndrome
  • History of seizures, epilepsy, stroke or head injury
Show all 9Show fewer
  • Metal implants
  • Pregnancy or considering pregnancy in near future
  • Body mass >/= 100kg

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Mediplex Health Care Center

    Rawalpindi, Punjab Province, 46060

Other trials in Pakistan

About this study

Official title: Effects of Core Strengthening Versus Motor Control Training on Pain, Disability & Endurance in Patients With Low Back Pain

The study aims to compare the effects of core strengthening versus motor control training on pain, disability \& endurance in patients with low back pain

Read the detailed description

The study aims to compare the effects of core strengthening versus motor control training on pain, disability \& endurance in patients with low back pain.

Comparing core strength and conditioning versus motor control for low back pain on physical and self-report outcomes lies in identifying the most effective treatment approach for this condition. This will help to determine which one yields better results in terms of improving physical function and reducing self-reported pain and disability associated with low back pain. This study can provide valuable insights for clinicians and patients in selecting the most appropriate treatment option.

Conditions
Low Back Pain
Being tested
Core Strengthening Exercises, Motor Control Training
Keywords
back pain, disability, endurance, core strengthening, motor control
Medical subject headings
Low Back Pain, Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Core Strengthening ExercisesOther

    The Core Strengthening Program participants will have supervised gym-based sessions for 8 weeks. In the first 4 weeks , participants will attend two 1 hour training sessions, followed by self-selected one or two sessions per week. The session will begin with 20min of aerobic conditioning of walking or running on a treadmill, starting at 65% and moving to 85% of HR max. The 5 key elements of focus are i. Centering ii. Breathing iii. Head and neck placement iv. Shoulder placement v. Chest wall placement

  • Motor Control TrainingOther

    Participants in Motor Control group will receive two physiotherapy sessions of 1hour / week in the first 4 weeks, during stage 1. i. Abdominal drawing-in maneuver (ADIM) : isometric contraction of the local stability muscles (e.g., lumbar multifidus, transversus abdominis) in minimally loading positions (supine lying, quadruped, sitting, and standing) by maintaining a neutral spine while maintaining normal breathing. During Phase 2, One 1 hour session / week in the second 4 weeks.

    Activation and facilitation of transversus abdominis, lumbar multifidus and pelvic floor motor control(36).Exercises target the transversus abdominis, multifidus and pelvic floor muscles plus postural correction to restore optimal motor control during non-weight-bearing activities. Exercises and progressions will follow previous protocols of motor control exercise.

Study groups in NCT06756685
Study groupRoleWhat they receive
Core Strengthening ExercisesExperimentalCore Strengthening Exercises
Receives: Other: Core Strengthening Exercises
Motor Control TrainingActive comparatorMotor Control Training
Receives: Other: Motor Control Training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Goniometer

    A goniometer will be used to measure ranges of motion of Trunk in Flexion, Extension, lateral Flexion and Rotation

    Measured: 8 weeks

  2. Lower body strength

    One-repetition maximum (1-RM) leg press at 70% 1-RM will be used to evaluate lower body strength.

    Measured: 8 weeks

  3. Modified Oswestry disability index

    The Oswestry Disability Index is considered one of the best accepted tools for assessment of low back pain. It is a patient-completed questionnaire which gives a subjective percentage score of level of function (disability) in activities of daily living in chronic low back pain. The ODI is made up of 10 items. Each item consist of 6 statements which are scored from 0 to 5. With 0 indicating the least disability and 5 the greatest then the total score is calculated as a percentage, with 0% indicating no disability and 100% indicating the highest level of disability.

    ODI = (Sum of items scored/Sum of sections answered) X 100

    Measured: 8 weeks

  4. Tampa scale of kinesiophobia

    The Tampa Scale of Kinesiophobia (TSK) was first developed in 1991 by R. Miller, S. Kopri, and D. Todd. A self-reported questionnaire that quantifies fear of movement, or (re)injury.It uses a 4-point Likert scale (Strongly Disagree-Disagree-Agree-Strongly Agree).The 17 item TSK total scores range from 17 to 68 where the lowest 17 means no or negligible kinesiophobia, and the higher scores indicate an increasing degree of kinesiophobia.Scores above 37 (17-item) are generally considered to indicate kinesiophobia.

    Measured: 8 weeks

  5. Visual analog scale

    The pain VAS is a uni dimensional measure of pain intensity, used to record patients' pain progression, or compare pain severity.Using a ruler, the score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100. A higher score indicates greater pain intensity.no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm).Test-retest reliability has been shown to be good and moderate to good reliability for disability in patients with chronic musculoskeletal pain.

    Measured: 8 weeks

  6. Japanese orthopedic association back pain evaluation questionnaire

    The JOABPEQ includes twenty-five questions that are subdivided into five sub scales: lower back pain, lumbar function, walking ability, social life function, and mental health. These questions are Intended to evaluate individuals with low back pain from five different perspectives.scores range from 0 to 100, with higher scores indicating a better patient condition. Both kappa and weighted kappa were more than 0.50 for all but one item, which was 0.48.

    Measured: 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Jan 2025
  2. Study start7 Aug 2024
  3. Primary completion1 Jan 2025
  4. Study completion10 Jan 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
74 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06756685
Sponsor's protocol ID
014384/Sabiha Fayyaz
Status last verified
Aug 2025
First submitted
13 Aug 2024
Last updated
29 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Core Strengthening Exercises in people with Low Back Pain, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Goniometer (time frame: 8 weeks). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Aug 2025.

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