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

April 28, 2026 updated by: Minna Stolt, University of Turku

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

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.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

107

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Southwest Finland
      • Turku, Southwest Finland, Finland, 20520
        • University of Turku

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

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

Exclusion Criteria:

  • Nursing students

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: 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.
Foot(at)Work intervention is targeted for nurses working in clinical settings to promote their competence in lower extremity health self-care.
No Intervention: Control group
The control group will work and live as usual.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge of lower extremity self-care
Time Frame: before intervenion, right after the intervention, one, six and 12 months after the intervention
Knowledge will be measured with self-administered questionnaira that contains 20 items (response options yes-no) about self-care for lower extremity problems.
before intervenion, right after the intervention, one, six and 12 months after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-assessed foot health
Time Frame: before intervenion, right after the intervention, one, six and 12 months after the intervention
Self-Administered Foot Health Assessment Instrument (S-FHAI) will measure subjective self-assessment measure of current foot health with 22 items. Four subcategories were included: skin health (12 items), nail health (4 items), foot structure (5 items), and foot pain (1 item).
before intervenion, right after the intervention, one, six and 12 months after the intervention
Musculoskeletal health
Time Frame: before intervenion, right after the intervention, one, six and 12 months after the intervention
Nordic Musculoskeletal Questionnaire will be used as self-report measure to assess the impact of a musculoskeletal condition on an individual's functioning and on the impact of the condition on daily activities.
before intervenion, right after the intervention, one, six and 12 months after the intervention
Self-perceived work ability
Time Frame: before intervenion, right after the intervention, one, six and 12 months after the intervention
Work ability index: one question where respondent indicates the level of perceived current work ability. Range 1-10 where 1 indicates not capable of working - 10 best possible work ability.
before intervenion, right after the intervention, one, six and 12 months after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 15, 2024

Primary Completion (Actual)

December 31, 2025

Study Completion (Actual)

December 31, 2025

Study Registration Dates

First Submitted

August 12, 2024

First Submitted That Met QC Criteria

August 12, 2024

First Posted (Actual)

August 15, 2024

Study Record Updates

Last Update Posted (Actual)

May 5, 2026

Last Update Submitted That Met QC Criteria

April 28, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 230374

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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