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The pain-relief effect of virtual reality technology in continuous passive motion training during burn patient rehabilitation

The pain-relief effect of virtual reality technology in continuous passive motion training during burn patient rehabilitation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129501
Enrollment
Unknown
Registered
2026-08-05
Start date
2026-08-10
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Burn

Interventions

Sequence A:First cycle: continuous passive motion training (CPM)+ virtual reality technology (VR)
second cycle: regular CPM
Sequence B:First cycle: regular CPM
second cycle: CPM + VR

Sponsors

The 969th Hospital of the Joint Logistics Support Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–70 years, any gender; 2. Clearly diagnosed as a patient in the post-burn recovery phase; 3. At least one joint needs CPM training; 4. Vital signs are stable and able to cooperate with CPM rehabilitation training; 5. Conscious, able to understand the study and complete the NRS pain score; 6. Expected to complete two CPM training sessions for the same joint with the same parameters, each lasting 15 minutes; 7. Willing to participate in this study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe vision or hearing impairment that prevents the use of VR equipment; 2. History of epilepsy, photosensitive epilepsy, severe motion sickness, or severe vertigo; 3. Facial or head wounds, dressings, external fixation, or tubes that affect wearing VR equipment; 4. Unstable fractures, joint dislocations, severe infections, unstable graft areas, or other conditions in the training area that make movement unsafe; 5. Pain medication plan is expected to be inconsistent over two study cycles; 6. Pregnant or breastfeeding women; 7. Other situations where the researcher thinks participation in this study is not suitable.

Design outcomes

Primary

MeasureTime frame
The worst NRS score during the CPM training process;

Secondary

MeasureTime frame
Resting pain before CPM training;Pain before CPM training;Average pain NRS during the CPM training process, which is the average of the pain scores at 5, 10, and 15 minutes;Pain change value: Most painful NRS during training ? Resting pain NRS before training;Use of rescue pain medication in the first 6 hours before CPM and within 2 hours after CPM;Training tolerance NRS score;Anxiety and subjective experience;Heart rate, blood pressure;Joint mobility before and after training;

Countries

China

Contacts

Public ContactJiachen Fu

The 969th Hospital of the Joint Logistics Support Force

1103000071@qq.com+86 176 2929 1103

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026