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Construction and preliminary application of E-coach self-management intervention program for patients with arteriosclerosis occlusion disease

Construction and preliminary application of E-coach self-management intervention program for patients with arteriosclerosis occlusion disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300079329
Enrollment
Unknown
Registered
2023-12-31
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Arteriosclerosis occlusion disease

Interventions

Experimental group:The intervention group will implement an E-Coach home-based exercise self-management intervention program based on routine exercise care.

Sponsors

Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) ASO patients were diagnosed according to the ASO guidelines. Diagnostic criteria: ? Age> 40 years; ? Smoking, diabetes, hypertension, hyperlipidemia and other high-risk factors; ? Clinical manifestations of ASO of the lower limbs; ? The distal artery pulse of the ischemic limb is weakened or disappeared; ?ABI=0.9; ? Color Doppler ultrasound, CTA, MRA and DSA showed lesions such as stenosis or occlusion of the corresponding artery, The first 4 patients can make the clinical diagnosis of lower limb ASO; (2) Judging by two attending physicians who have worked for 10 years or more, Patients with successful interventional procedures (residual vascular stenosis <30%); (3) After treatment, the condition was stable and discharged from hospital; (4) Clear awareness, Cognition is normal; (5) Patients or main caregivers can use smart phones to surf the Internet and send and receive information; (6) Informed consent from patients and primary caregivers, Voluntary participation.

Exclusion criteria

Exclusion criteria: (1) severe dysfunction such as heart, brain, kidney and other important organs; (2) amputation due to disease; (3) patients with mental and neurological diseases; (4) life expectancy <1 year; (5) patients who have participated in other home-based intervention trials.

Design outcomes

Primary

MeasureTime frame
The 6-min walk test distance;

Secondary

MeasureTime frame
Score of Patient Self-management Assessment Scale after ASO intervention;Maximum painless walking time;VascuQol-6;The Family Support Function Scale;Major adverse cardiovascular events, amputation rates, and mortality rates;

Countries

China

Contacts

Public ContactWang Dan

Affiliated Hospital of Southwest Medical University; Southwest Medical University

2366552187@qq.com+86 138 8270 1643

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026