- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06555198
Promotion of Nurses' Lower Extremity Health by Foot(at)Work Intervention (Foot(at)Work)
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
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Southwest Finland
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Turku, Southwest Finland, Finland, 20520
- University of Turku
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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.
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Foot(at)Work intervention is targeted for nurses working in clinical settings to promote their competence in lower extremity health self-care.
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No Intervention: Control group
The control group will work and live as usual.
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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).
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before intervenion, right after the intervention, one, six and 12 months after the intervention
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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.
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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.
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before intervenion, right after the intervention, one, six and 12 months after the intervention
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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