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Effectiveness of Health Belief Model-based ankle-foot training combined with transcutaneous acupoint electrical stimulation in diabetic high-risk foot patients

Effectiveness of Health Belief Model-based ankle-foot training combined with transcutaneous acupoint electrical stimulation in diabetic high-risk foot patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127709
Enrollment
Unknown
Registered
2026-07-06
Start date
2026-07-08
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

High-Risk Diabetic Foot

Interventions

Intervention group:In order to carry out intervention for high-risk diabetic foot patients based on the foot and ankle training and acupoint electrical stimulation intervention plan constructed in the
Control group:Routine care, specific implementation plan: It will be carried out through offline small lectures and distribution of promotional brochures to enable patients to understand the risk fact
Guide patients on how to properly perform self-foot care, such as warm water baths and foot massages. Knowledge about correctly choosing shoes, socks and trimming toenails
How to deal with corns, calluses, etc.

Sponsors

The Affiliated Hospital, Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for T2DM according to the Guidelines for the Prevention and Treatment of Diabetes in China (2024 Edition) formulated by the Chinese Diabetes Society. 2.Meet the definition of high-risk diabetic foot (presence of peripheral neuropathy without diabetic foot ulcers). 3. Age: 18–75 years. 4. Clinically stable, able to understand and willing to comply with the study procedures.

Exclusion criteria

Exclusion criteria: 1. Patients with acute diabetic complications, concurrent acute infections, proliferative retinopathy, severe nephropathy, severe cardiovascular or cerebrovascular diseases, or a history of malignant tumors, etc. 2. Patients with bone, joint, or muscle disorders that make them unsuitable for exercise. 3. Patients with recurrent hypoglycemia or significant blood glucose fluctuations. 4. Patients with contraindications to transcutaneous electrical stimulation, such as having an implanted cardiac pacemaker, local skin damage or infection at the treatment site, or allergy to electrode pads.

Design outcomes

Primary

MeasureTime frame
Michigan neuropathy screeninginstrument;Gait parameters;

Secondary

MeasureTime frame
General Information Questionnaire;Quality of life scale for patients with type2 diabetes mellitus;Self-efficacy for exercise;Five times sittingand standing test ;Adverse event;

Countries

China

Contacts

Public ContactLiu Li

Department of Hematopathology, The Affiliated Hospital, Southwest Medical University

18715820552@163.com+86 187 1582 0552

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026