NCT07466680

Brief Summary

The goal of this feasibility study is to learn if a work environment program to address musculoskeletal disorders and pain, can be implemented and accepted by employees with physical demanding work tasks. The main question it aims to answer is:

  • Will the intervention be accepted by the workers?
  • It it feasible to implement a workplace intervention to prevent musculoskeletal disorders and pain? Participants will:
  • Implement the intervention
  • Participate in the intervention twice a week for eight weeks
  • Answer questionnaires and participate in interviews to evaluate the intervention

Trial Health

87
On Track

Trial Health Score

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

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable pain

Timeline
Completed

Started Apr 2025

Shorter than P25 for not_applicable pain

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 10, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 27, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 27, 2025

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

March 3, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

March 12, 2026

Completed
Last Updated

March 12, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

March 3, 2026

Last Update Submit

March 7, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Acceptability

    The theoretical framework of acceptability questionnaire will be used to evaluate acceptability as well as interviews guided by the acceptability framework.

    From enrollment to the end of the 10 week-intervention period

Study Arms (1)

GLAD intervention

OTHER
Behavioral: GLAD intervention

Interventions

The intervention consists of two components: 1. Implementation of the GLAD intervention to the workers at one unit at the participating workplaces. The GLAD intervention consists of 15 modules containing knowledge on pain, participatory ergonomics and physical exercises. Each module last 30 minutes and are delivered by an occupational safety and health professional (OSH). 2. Education of the OSH's to deliver the GLAD intervention. The education aim to give the OSH the necessary knowledge, skills and competencies to deliver the intervention to the workers at their workplaces. The education program consists of evidence-based knowledge on pain and management, content of the GLAD intervention and implementation strategies. The education is delivered as an online preparatory work (approximately 1 hour) and a 7-hour course with physical attendance.

GLAD intervention

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • An in-house occupational safety and health professional (OSH) employed at the workplace, or an out-house OSH employed at one of two OSH consultancies.
  • All the workers employed at the unit at the participating workplace.

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The National Research Centre for the Working Environment

Copenhagen, Denmark

Location

MeSH Terms

Conditions

PainMusculoskeletal Diseases

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 3, 2026

First Posted

March 12, 2026

Study Start

April 10, 2025

Primary Completion

June 27, 2025

Study Completion

June 27, 2025

Last Updated

March 12, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations