NCT07385833Completed
Disaster Preparedness in Patients With Diabetic Foot: The Effect of an Educational Intervention
Source: ClinicalTrials.gov · Last updated 4 Feb 2026
Brief summary (registry, in English)
This quasi-experimental study aims to evaluate the effect of a disaster preparedness education program on disaster preparedness levels, foot care behaviors, and diabetic foot care self-efficacy in patients with type 2 diabetes diagnosed with diabetic foot. Participants are assigned to an intervention group receiving structured education on diabetic foot management and disaster preparedness, or to a control group receiving routine care. Outcomes are assessed at baseline, post-intervention, and follow-up.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 68 (actual)
- First submitted
- 26 Jan 2026
- Start date
- 1 Feb 2024
- Primary completion date
- 1 May 2024
- Lead sponsor
- Senem Duman
- Diseases
- Type 2 diabetes
- NCT number
- NCT07385833
What you commit to
- Study type: Interventional
- Participants enrolled: 68
- From 1 Feb 2024 to the primary completion date, 1 May 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- • History of diabetic foot-related amputation
- Presence of active Charcot neuroarthropathy
- Severe cognitive impairment affecting participation
- Significant communication barriers preventing completion of assessments
- Presence of acute medical conditions requiring immediate intensive treatment during the study period
Who the study is looking for
- • Diagnosed with type 2 diabetes mellitus for at least 6 months
- Diagnosed with diabetic foot classified as Wagner grade 1, 2, or 3
- Receiving outpatient or inpatient care at the diabetic foot center
- Able to communicate and complete self-report questionnaires
- Willing to participate and provide written informed consent
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ankara Etlik City Hospital Coordinator of this site? Confirm its status | Ankara | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.