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A Multicenter Clinical Study on the Evaluation of Psychosomatic Status and the Efficacy of Mindfulness-Based Intervention in Chinese Patients with Spinal Cord Injury

A Multicenter Clinical Study on the Evaluation of Psychosomatic Status and the Efficacy of Mindfulness-Based Intervention in Chinese Patients with Spinal Cord Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111437
Enrollment
Unknown
Registered
2025-10-31
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Spinal Cord Injury

Interventions

Trial Group:The intervention group will receive a combined strategy consisting of remote mindfulness-based therapy and standard rehabilitation training. The mindfulness therapy comprises 8 sessions in
Control Group:The control group will receive standard post-operative rehabilitation training for spinal cord injury alone, without the remote mindfulness therapy component.

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients within two years after thoracolumbar spinal cord injury. 2.Ability to maintain basic living with substantial assistance and care from others. 3.Life expectancy greater than 1 year. 4.Agreement to participate in the study and provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients who have previously undergone a mindfulness-based intervention. 2.Patients who have been diagnosed with major depressive disorder and require pharmacological treatment. 3.Patients who present with neurological dysfunction that is not caused by spinal cord injury. 4.Patients who are unwilling to undergo the study assessments and procedures. 5.Patients who are currently participating in another clinical drug trial or interventional research. 6.Patients who have severe comorbidities in major organ systems or are judged by the physician as unable to participate in the assessments.

Design outcomes

Primary

MeasureTime frame
Quality of Life;

Secondary

MeasureTime frame
Spinal Cord Lesion Independence;Depression Status;Anxiety Status;Post Traumatic Growth;neurological function;Physical Pain Status;Safety;

Countries

China

Contacts

Public ContactCheng Liming

Shanghai Tongji Hospital

limingcheng@tongji.edu.cn+86 137 0195 9550

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 28, 2026