Learning to prepare: study tests disaster readiness for diabetic foot patients
NCT ID NCT07385833
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a special education program could help people with diabetic foot (a serious complication of type 2 diabetes) become more prepared for disasters like earthquakes or floods. 68 patients took part, with some receiving the education and others getting usual care. The goal was to see if the program improved their disaster readiness, foot care habits, and confidence in managing their condition.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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68 people
The number who actually took part.
- Started
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Feb 2024
- Finished
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Jan 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * • 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 Exclusion Criteria: * • 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ankara Etlik City Hospital
Ankara, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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