Promotion of Nurses' Lower Extremity Health by Foot(at)Work Intervention (NCT06555198) | Clinical Trial Compass
CompletedNot Applicable
Promotion of Nurses' Lower Extremity Health by Foot(at)Work Intervention
Finland107 participantsStarted 2024-10-15
Plain-language summary
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.
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Registered nurse
* Working in the specialized health care in surgical or internal medicine wards of one certain hospital
Exclusion Criteria:
* Nursing students
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial focused on nurses' foot and lower extremity health through an educational program — could a similar self-care knowledge approach be useful for my own lower extremity or foot problems, and are there comparable programs my doctor could point me to?
2Since this study measured whether participants gained knowledge about lower extremity self-care rather than directly tracking clinical outcomes like pain reduction or structural improvement, does that mean the evidence it produces is still quite early-stage, and what would my doctor consider stronger evidence for treating my specific foot condition?
3The trial is now completed — is there any published data or results from it that my doctor could review to see whether the self-care education strategies tested might be relevant to managing my situation?
4Given that this intervention was designed specifically for nurses as an occupational group, how much of what was studied would actually translate to my own circumstances, and are there foot or lower extremity care programs better matched to my lifestyle and diagnosis?
5Before looking at trial-based approaches, would my doctor recommend starting with established standard treatments for my foot deformity or lower extremity problem, and how would we know if those aren't working well enough to consider something different?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Knowledge of lower extremity self-care
Timeframe: before intervenion, right after the intervention, one, six and 12 months after the intervention