NCT07177040

Brief Summary

Non-specific low back pain (NSLBP) is extensively musculoskeletal conditions, where manual therapy techniques have been widely employed in its management, but their short term efficacy in chronic low back pain still need more investigations. Objective: This study aimed to discuss the SNAG versus Maitland techniques in the management of NSLBP. Methods: 60 patients with chronic NSLBP will share in the study. Sessions will be conducted 3 times per week for 4 weeks. The outcomes will be evaluated for pain by the numerical rating pain scale (NPRS), disability through Oswestry Disability Index, flexion range of motion by back range of motion device, postural stability by Biodex system will be assessed at baseline, immediately post-intervention, and at a four-week follow-up

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

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

First Submitted

Initial submission to the registry

September 9, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 16, 2025

Completed
19 days until next milestone

Study Start

First participant enrolled

October 5, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2025

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2026

Completed
Last Updated

October 7, 2025

Status Verified

September 1, 2025

Enrollment Period

3 months

First QC Date

September 9, 2025

Last Update Submit

October 2, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Numeric Pain Rating Scale

    The NPRS will be used to evaluate the level of pain by selecting a number on a rating scale, ranging from 0 (no pain) to 10 (worst and unbearable pain).

    4 weeks

Secondary Outcomes (3)

  • Functional disability

    4 weeks

  • Lumbar flexion range of motion

    4 weeks

  • overall stability index (OSI)

    4 weeks

Study Arms (2)

Maitland

ACTIVE COMPARATOR

Participants will receive Maitland technique therapy

Procedure: MaitlandProcedure: SNAG

SNAG

ACTIVE COMPARATOR

Participants will receive SNAG therapy based on the Mulligan Concept

Procedure: MaitlandProcedure: SNAG

Interventions

MaitlandPROCEDURE

Maitland technique therapy, which consists of passive mobilizations applied to the lumbar facet joints in an anterocranial direction while the patient is in a prone lying position

MaitlandSNAG
SNAGPROCEDURE

The technique involves applying a sustained glide to the lumbar facet joints while the patient is in a sitting position, and the pelvic girdle will be stabilized by a belt. Then the therapist will ask the patient for active forward flexion of the spine while the pressure on the facet joint is maintained during the movement till its end

Also known as: sustained natural apophyseal glide
MaitlandSNAG

Eligibility Criteria

Age25 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Adults aged 25 to 40 years.
  • Diagnosed with chronic NSLBP persisting for more than three months.
  • Pain intensity between 3 to 6 on the Visual Analog Scale (VAS) during lumbar extension in a sitting position.
  • Oswestry Disability Index (ODI) score between 20% to 40%.
  • Restriction of the movement only in flexion ROM with the ability to perform at least 40° of trunk flexion.

You may not qualify if:

  • Specific causes of low back pain (e.g., herniated disc, spinal stenosis).
  • History of spinal surgery or trauma.
  • Neurological deficits or systemic diseases affecting the musculoskeletal system.
  • Pregnancy.
  • Current participation in other physiotherapy programs.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Medical Clinics

Hail, 0000, Saudi Arabia

Location

Central Study Contacts

Ehab Ahmed, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Department of Public Health, College of Public Health and Health Informatics, University of Hail, Ha'il, Saudi Arabia

Study Record Dates

First Submitted

September 9, 2025

First Posted

September 16, 2025

Study Start

October 5, 2025

Primary Completion

December 30, 2025

Study Completion

January 20, 2026

Last Updated

October 7, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

All the data will be obtained from the experiment is under the protection of the Scientific Research Deanship, University of Ha'il, Saudi Arabia as this project is funded from it with number RG-20 202.

Locations