Promotion of Nurses' Lower Extremity Health by Foot(at)Work Intervention

NCT ID: NCT06555198

Last Updated: 2025-03-30

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

160 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-15

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The quasiexperimental study aims to analyse the effecs of Foot(at)Work intervention on nurses' lower extremity health. The Foot(at)Work intervention is in electronic format consisting of 5 themes. The idea is that the participants familiarizes with the foot health -related content. The primary outcome is knowledge about lower extremity self-care. Secondary outcomes are work well-being, lower extremity health and musculoskeletal health. The outcomes are measured before the intervention (M0), after the intervention (M1), one month after the intervention (M2), six months after the intervention (M3) and 12 months after the intervention (M4).

The purpose of the Foot(at)Work intervention is to support nurses ability to self-care their lower extremities. The intervention consists of text, videos, and pictures that educate nurses to self-care their lower extremities and to select proper footwear.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Lower Extremity Problem Foot Deformities

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intervention group

Foot(at)Work intervention will be offered to participant sin the intervention group. The Foot(at)Work intervention lasts for 5 weeks. The intervention is constructed on electronic learning environment consisting of 5 themes illustrating self-care activities for common foot problems among nursing professionals. The idea of self-directed learning is to support nurses competence to self-care their lower extremities and thus, promote their work wellbeing in clinical nursing environments.

Group Type EXPERIMENTAL

Foot(at)Work intervention

Intervention Type BEHAVIORAL

Foot(at)Work intervention is targeted for nurses working in clinical settings to promote their competence in lower extremity health self-care.

Control group

The control group will work and live as usual.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Foot(at)Work intervention

Foot(at)Work intervention is targeted for nurses working in clinical settings to promote their competence in lower extremity health self-care.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Registered nurse
* Working in the specialized health care in surgical or internal medicine wards of one certain hospital

Exclusion Criteria

* Nursing students
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

The Hospital District of Satakunta

OTHER

Sponsor Role collaborator

Finnish Work Environment Fund

OTHER

Sponsor Role collaborator

University of Turku

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Minna Stolt

professor (act.), PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Turku

Turku, Southwest Finland, Finland

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Finland

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Minna Stolt, Dr., Prof.

Role: CONTACT

-358469237973

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Minna Stolt

Role: primary

+358469237973

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

230374

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Foot Self-care in Older Adults
NCT03656341 COMPLETED NA