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Construct and feasibility study of nursing intervention based on behavior change wheel theory on rehabilitation effectiveness of clubfoot patients

Construct and feasibility study of nursing intervention based on behavior change wheel theory on rehabilitation effectiveness of clubfoot patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098434
Enrollment
Unknown
Registered
2025-03-07
Start date
2024-12-01
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Club foot

Interventions

Intervention group - control group:The trial receives interventions based on BCW theory, selecting appropriate intervention functions in terms of motivation, ability and opportunity. These included re
Control subjects:Disease-related information, preoperative preparation, psychological care, dietary care, muscle training, pain management, use of supportive frames, care of external fixators, rehabil

Sponsors

Beijing Rehabilitation Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Meets the diagnostic criteria of the International Foot Association for clubfoot; 2.Patients aged 13-40 years old; 3.All patients underwent Ilizarov technique for surgical treatment; 4.The patient has normal expression ability and is able to communicate effectively; 5.The patient signs an informed consent form and is willing to participate and cooperate in this study.

Exclusion criteria

Exclusion criteria: 1.Patients with conscious and cognitive impairments; 2.Patients with other serious systemic diseases (such as severe heart, lung, liver, kidney and other important organ dysfunction) that may affect the evaluation of rehabilitation efficacy or intervention implementation. 3.Patients with severe infections, ulcers, or other skin lesions on the feet that are not suitable for rehabilitation interventions; 4.Patients who are currently participating in other clinical studies that may affect the results of this study. 5.Individuals with poor overall health and inability to tolerate surgery;

Design outcomes

Primary

MeasureTime frame
ICFSG;

Secondary

MeasureTime frame
SF- -36;Anxiety;GSES score;

Countries

China

Contacts

Public ContactKang Jie

Beijing Rehabilitation Hospital Affiliated to Capital Medical University

1034476573@qq.com+86 134 8867 1022

Outcome results

None listed

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