Skip to content

Preliminary Study on the Effectiveness of Diafootcare

An Exploratory Clinical Trial to Assess the Efficacy of DiaFootCare

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0012091
Enrollment
36
Registered
2026-06-08
Start date
2025-09-18
Completion date
Unknown
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : This is an exploratory clinical study designed to investigate the effects of a self-management intervention for patients with diabetic foot conditions using a mobile application. It is a

Sponsors

Yonsei University, Wonju Severance Christian Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Among patients visiting the outpatient clinics of Orthopedic Surgery and Endocrinology, those who meet the following inclusion criteria will be eligible for participation: - Adults aged 19 years or older - Patients diagnosed with diabetes who have developed diabetic foot ulcers - Patients currently receiving treatment for diabetic foot ulcers - Patients who have undergone amputation surgery due to diabetic foot ulcers - Patients receiving postoperative management and treatment for recurrence prevention - Patients presenting with one or more of the following conditions: *Loss of protective sensation: Patients with sensory impairment confirmed by a 10 g monofilament test *Peripheral vascular disease: Patients with weak or absent pedal pulses *Poor glycemic control: Patients with elevated HbA1c levels indicating inadequate blood glucose control *History of foot ulceration: Patients with a previous history of foot ulcers *Foot deformity: Patients with toe deformities, calluses, or other structural abnormalities *Smoking: Patients who currently smoke or have a history of smoking *Impaired renal function: Patients with chronic kidney disease

Exclusion criteria

Exclusion criteria: -Participants under the age of 19 -Individuals with impaired decision-making capacity -Individuals who do not provide consent to participate in the clinical trial -Individuals deemed unsuitable for participation by the principal investigator (orthopedic specialist) -Individuals who have difficulty using general-purpose devices such as smartphones

Design outcomes

Primary

MeasureTime frame
Satisfaction with user; Application usage/adherence (compliance);Fasting blood sugar

Secondary

MeasureTime frame
Depression screening assessment (Patient Health Questionnaire-9);Confidence / Self-efficacy;Perceived changes in self-management and health behaviors

Countries

Korea, Republic of

Contacts

Public ContactHEEJIN KIM

Yonsei University, Wonju Severance Christian Hospital

dhheejin@yonsei.ac.kr+82-33-741-0114

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Jun 21, 2026