Lumbar Support Belt for Low-Back Pain in Office Workers

NCT ID: NCT07030816

Last Updated: 2025-06-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-01

Study Completion Date

2024-04-30

Brief Summary

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Background:

Low-back pain (LBP) is common among office workers and can reduce productivity and quality of life. Lumbar support belts are commonly used to manage LBP, but their effectiveness specifically for office workers remains uncertain.

Aim:

This study investigates whether wearing a commercially available lumbar support belt (Guardner Belt) can reduce low-back pain, decrease physical fatigue during computer work, and improve perceived work performance among office workers with chronic low-back pain.

Methods:

Thirty office workers with chronic nonspecific low-back pain were randomly assigned to either wear the lumbar support belt during work hours for four weeks or continue usual activities without the belt. Participants' pain, fatigue, and work performance were assessed before and after the intervention period.

Detailed Description

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Study Design:

A single-centre, open-label, parallel-group randomised controlled trial conducted at a logistics company in Okinawa, Japan.

Participants:

Inclusion criteria: full-time office workers aged 20 to 65 years, chronic nonspecific low-back pain intensity ≥ 30 mm (100-mm visual analogue scale; VAS).

Exclusion criteria: prior lumbar surgery, ongoing pharmacologic treatment for low-back pain, anticipated changes in job duties during the trial period.

Interventions:

* Belt Group: Participants wore a commercially available elastic lumbar support belt (Guardner Belt) sized according to waist circumference. Participants were instructed to wear the belt for at least 8 hours daily during their working hours over a 4-week period.
* Control Group: Participants continued normal daily routines without any lumbar support belt.

Primary Outcome Measures:

Assessed at baseline and after 4 weeks of intervention:

* Low-back pain intensity: Measured using a 100-mm Visual Analogue Scale (VAS).
* Physical fatigue during computer work: Measured using a 100-mm VAS.
* Work performance: Measured using the Single-Item Presenteeism Question (SPQ), scored from 0% (no productivity) to 100% (full productivity).

Ethics:

Ethical approval was retrospectively granted by the Ryusei Hospital Institutional Review Board (Approval Number 202502). Written informed consent was obtained from all participants.

Conditions

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Low Back Pain (LBP) Chronic Low Back Pain Non-specific Low Back Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Lumbar Support Belt Group

Participants wore a commercially available elastic lumbar support belt (Guardner Belt) sized according to waist circumference during working hours (≥ 8 hours/day) for 4 weeks.

Group Type EXPERIMENTAL

Guardner Belt

Intervention Type DEVICE

The Guardner Belt is a commercially available elastic lumbar support belt designed to reduce low-back pain and improve posture. Participants wore the belt sized according to waist circumference for at least 8 hours per day during working hours for 4 weeks.

Control Group

Participants continued their usual daily work routines without using any lumbar support belt.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Guardner Belt

The Guardner Belt is a commercially available elastic lumbar support belt designed to reduce low-back pain and improve posture. Participants wore the belt sized according to waist circumference for at least 8 hours per day during working hours for 4 weeks.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* • Full-time desk workers

* Chronic nonspecific low-back pain (≥30 mm on a 100-mm visual analogue scale at baseline)
* Age between 20 and 65 years

Exclusion Criteria

* • Previous lumbar surgery

* Currently receiving pharmacologic treatment for low-back pain
* Planned job-duty changes during the study period
Minimum Eligible Age

20 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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General Incorporated Foundation Ryukyuseimeisaiseikai, Ryusei Hospital.

OTHER

Sponsor Role lead

Responsible Party

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Shinyu Kise

Principal Investigator , Institute for Tourism and Health

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ryusei Hospital

Naha, Okinawa, Japan

Site Status

Countries

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Japan

References

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Qaseem A, Wilt TJ, McLean RM, Forciea MA; Clinical Guidelines Committee of the American College of Physicians; Denberg TD, Barry MJ, Boyd C, Chow RD, Fitterman N, Harris RP, Humphrey LL, Vijan S. Noninvasive Treatments for Acute, Subacute, and Chronic Low Back Pain: A Clinical Practice Guideline From the American College of Physicians. Ann Intern Med. 2017 Apr 4;166(7):514-530. doi: 10.7326/M16-2367. Epub 2017 Feb 14.

Reference Type BACKGROUND
PMID: 28192789 (View on PubMed)

Other Identifiers

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202502

Identifier Type: -

Identifier Source: org_study_id

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