NCT07683676

Brief Summary

This study will be conducted to comapre between kinetic control training versus core stability exercises on proprioception and spatiotemporal gait parameters in chronic non-specific low back pain.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P50-P75 for not_applicable low-back-pain

Timeline
9mo left

Started Jul 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress8%
Jul 2026May 2027

First Submitted

Initial submission to the registry

June 8, 2026

Completed
28 days until next milestone

First Posted

Study publicly available on registry

July 6, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

July 10, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2027

Last Updated

July 6, 2026

Status Verified

July 1, 2026

Enrollment Period

10 months

First QC Date

June 8, 2026

Last Update Submit

July 1, 2026

Conditions

Keywords

Kinetic ControlCore Stability ExercisesProprioceptionSpatiotemporal Gait ParametersChronic Non-specific Low Back Pain

Outcome Measures

Primary Outcomes (1)

  • lumber repositioning error (lumbar proprioception)

    The iPhone® application will be used to assess lumbar repositioning error. It will be placed vertically, halfway between the anterior superior and PSIS, just above the iliac crest, and fastened with a belt. The initial location and the inclination of the inclinometer were both fixed at 0°. There was a 0 to 30° range of motion (ROM). The assessor gently guided the individual to a 30° flexion and instructed them to hold this posture for ten seconds. After then, the participant actively went back to their starting location and subsequently did it three times.

    up to 8 weeks

Secondary Outcomes (7)

  • pain intensity

    up to 8 weeks

  • gait speed

    up to eight weeks

  • cadence

    up to eight weeks

  • stride and step time

    up to eight weeks

  • stride and step length

    up to eight weeks

  • +2 more secondary outcomes

Study Arms (3)

Kinetic control group

EXPERIMENTAL

Twenty patients will receive kinetic control training with conventional physical therapy three times a week for 8 weeks

Other: Kinetic control exercisesOther: conventional physical therapy

Core stability exercises group

EXPERIMENTAL

Twenty patients will receive core stability exercises with conventional physical therapy three times a week for 8 weeks

Other: Core stability exercisesOther: conventional physical therapy

Conventional physical therapy exercise

ACTIVE COMPARATOR

twenty patients will receive conventional physical therapy three times a week for 8 weeks

Other: conventional physical therapy

Interventions

Each patient in the group will be received kinetic control retraining with conventional physical therapy. For each movement direction, specific control tests will be conducted. The direction and site of the uncontrolled movement will be evaluated using special tests in accordance with the pain history of the patient.

Kinetic control group

Core stability exercises include curl up (head and shoulders lifting), bridging exercise with leg elevation, and quadruped with arm and leg lift will be performed with maintaining the lumbar spine neutral. each patient in that group will be received core stability exercises with conventional physical therapy,

Core stability exercises group

conventional physical therapy includes Trans-cutaneous electric Nerve Stimulation (TENS), Heat by hot packs

Conventional physical therapy exerciseCore stability exercises groupKinetic control group

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Subjects from both sexes diagnosed with chronic non-specific low back pain with uncontrolled movement related to kinetic control concept
  • aging range from 18-45 years
  • Pain provoked by movement.
  • Pain for at least 3 months
  • Pain with sufficient intensity (equal to or greater than 4 points on VAS).

You may not qualify if:

  • History of previous spinal surgery.
  • Patients with lumbar spine diseases (for example, disc prolapse or spondylolisthesis).
  • Patients with abnormal neurological signs in lower extremities, radicular pain in the lower limb, hip arthrosis, congenital musculoskeletal deformity, female patients with pelvic lesions, and pregnant females.
  • Red flag signs include unwanted weight loss, less than three months of symptom persistence, malignancies of the spine, spinal instability due to structural cause, for example: ligamentous sprain or spondylolisthesis.
  • Gynaecological problems in females that may cause low back pain include coccydynia and hysterotomy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Low Back Pain

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
obaque sealed envelope
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Kinetic Control Training Versus Core Stability Exercises
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator: Ola Adel Abd Elrazik Ibrahem

Study Record Dates

First Submitted

June 8, 2026

First Posted

July 6, 2026

Study Start

July 10, 2026

Primary Completion (Estimated)

May 1, 2027

Study Completion (Estimated)

May 1, 2027

Last Updated

July 6, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share