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The Effect of Individualized Rehabilitation Therapy Plans on Psychosocial Adaptation in Burn Patients

The Effect of Individualized Rehabilitation Therapy Plans on Psychosocial Adaptation in Burn Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116878
Enrollment
Unknown
Registered
2026-01-16
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Burn

Interventions

Intervention Group (Personalized Rehabilitation Therapy Plan):On the basis of conventional rehabilitation treatment, implement an individualized rehabilitation plan oriented towards psychosocial adapt
Control Group (Conventional Rehabilitation Protocol):Undergo routine treatment for burn rehabilitation

Sponsors

Mianyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=18 years, regardless of gender; 2.Meeting the diagnostic criteria for burns, with a total burn surface area (TBSA) >5%; 3.Clinically stable after burn injury, able to undergo rehabilitation therapy, and currently in the rehabilitation phase (scar formation stage or functional recovery stage); 4.Rehabilitation intervention (including early positioning, joint mobility training, and functional training) has been initiated or is about to begin; 5.Able to understand the study content and complete the relevant assessment scales, with the capacity to independently or with guidance complete questionnaires; 6.Voluntary participation in the study with signed informed consent.

Exclusion criteria

Exclusion criteria: 1.History of severe psychiatric disorder, severe cognitive impairment, or mental illness that would preclude cooperation with study assessments; 2.Severe dysfunction of major organs (e.g., heart, lung, liver, or kidney) or life-threatening complications; 3.Severe infection, persistent high fever, or other conditions unsuitable for rehabilitation training; 4.Concurrent participation in other interventional clinical trials; 5.Any other circumstances deemed by the investigators as inappropriate for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Hospital Anxiety and Depression Scale Score;

Secondary

MeasureTime frame
Brief Burn Specific Health Scale Score;Social Support Rating Scale Score;

Countries

China

Contacts

Public ContactTu Mei

Mianyang Central Hospital

252643731@qq.com+86 139 8110 9183

Outcome results

None listed

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