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Analysis of the current situation and influencing factors of exercise fear in patients with Lower extremity arterial Occlusive Disease after interventional surgery

Analysis of the current situation and influencing factors of exercise fear in patients with Lower extremity arterial Occlusive Disease after interventional surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127676
Enrollment
Unknown
Registered
2026-07-06
Start date
2026-07-07
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

Lower Extremity Arterial Occlusive Disease

Interventions

Observation Group:None

Sponsors

The First Affiliated Hospital of Army Medical University of the People's Liberation Army of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Those who have been diagnosed with lower extremity arterial occlusive disease through imaging examinations, with Fontaine stage II-IV, and have received interventional surgical treatment; 2. Those with normal and clear consciousness, good communication skills, and the ability to cooperate in completing questionnaires and scale assessments; 3. Those who are 18 years old or older, voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients undergoing hybrid surgery combining interventional and open surgery, acute limb ischemia, and secondary surgery; 2. Those with severe failure of vital organs such as the heart, liver, kidneys and brain; 3. Those with a history of cognitive dysfunction, mental illness, or who are unable to cooperate in completing the assessment; 4. Those who develop severe complications after the operation (such as massive hemorrhage, severe infection, limb necrosis, etc.) or have contraindications for exercise; 5. Those who refuse to participate in this study or withdraw halfway.

Design outcomes

Primary

MeasureTime frame
Kinesiophobia level after interventional surgery;The state where fear of movement occurs;

Secondary

MeasureTime frame
The degree of postoperative pain;Anxiety level;Depressive mood level;Level of medication compliance;Self-efficacy level;Level of social support;

Countries

China

Contacts

Public ContactZeng Yaqiong

The First Affiliated Hospital of Army Medical University of the People's Liberation Army of China

zyq930629@tmmu.edu.cn+86 23 68765761

Outcome results

None listed

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