NCT07801053

Brief Summary

This study compared the effectiveness of suspension exercises based on the Neurac method with conventional physiotherapy in adults with chronic non-specific low back pain. The study evaluated changes in pain intensity, health-related quality of life, and functional performance following a six-week intervention.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

January 15, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 26, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 26, 2026

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

August 28, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 3, 2026

Completed
Last Updated

September 3, 2026

Status Verified

August 1, 2026

Enrollment Period

5 months

First QC Date

August 28, 2026

Last Update Submit

August 28, 2026

Conditions

Treatment Adherence

Outcome Measures

Primary Outcomes (1)

  • Change in Pain Intensity Measured by the Visual Analogue Scale (VAS)

    Pain intensity was assessed using the Visual Analogue Scale (VAS). Change in pain intensity was evaluated by comparing the VAS score before and after the six-week intervention.

    Baseline and immediately after the 6-week intervention

Secondary Outcomes (2)

  • Change in Health-Related Quality of Life Measured by the Short Form-36 (SF-36)

    Baseline and immediately after the 6-week intervention

  • Change in Functional Performance Assessed by the Neurac Test Procedure

    Baseline and immediately after the 6-week intervention

Study Arms (2)

Suspension Exercise Group

EXPERIMENTAL

Participants received a standardized suspension exercise program based on the Redcord® Neurac method. The intervention consisted of 12 supervised treatment sessions delivered over a period of 6 weeks.

Behavioral: Suspension Exercises Using the Redcord® Neurac Method

Conventional Physiotherapy Group

ACTIVE COMPARATOR

Participants received a standardized conventional physiotherapy program consisting of thermotherapy, transcutaneous electrical nerve stimulation (TENS), manual therapy, therapeutic exercises, and a home exercise program. The intervention consisted of 12 supervised treatment sessions delivered over a period of 6 weeks.

Behavioral: Conventional Physiotherapy

Interventions

Conventional PhysiotherapyBEHAVIORAL

A standardized conventional physiotherapy program consisting of thermotherapy, transcutaneous electrical nerve stimulation (TENS), manual therapy, therapeutic exercises, and a home exercise program, delivered in 12 supervised treatment sessions over 6 weeks.

Conventional Physiotherapy Group
Suspension Exercises Using the Redcord® Neurac MethodBEHAVIORAL

A standardized suspension exercise program based on the Redcord® Neurac method, consisting of 12 supervised treatment sessions over 6 weeks.

Suspension Exercise Group

Eligibility Criteria

Age25 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • \. Adults aged 25 to 60 years with chronic non-specific low back pain.
  • \. No history of previous spinal surgery.
  • \. No history of major lumbar trauma.
  • \. Pain intensity of ≥3/10 on the Visual Analogue Scale (VAS).
  • \. Ability to understand the instructions and complete the questionnaires.
  • \. No previous participation in a suspension exercise program

You may not qualify if:

  • Recent lumbar trauma.
  • Spinal surgery performed less than six months before enrollment.
  • Pregnancy.
  • Severe cognitive or psychological disorders.
  • Refusal to participate.
  • Severe cardiovascular complications.
  • Acute joint pain limiting the ability to perform the exercises.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Motiongate clinic

Jounieh, Lebanon

Location

MeSH Terms

Conditions

Treatment Adherence and Compliance

Condition Hierarchy (Ancestors)

Health BehaviorBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

August 28, 2026

First Posted

September 3, 2026

Study Start

January 15, 2026

Primary Completion

June 26, 2026

Study Completion

August 26, 2026

Last Updated

September 3, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations

LE(1)