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A Study on the Application of a Virtual-to-Real Contextual Exercise Rehabilitation Program in Patients with Acute Exacerbation of COPD

A Study on the Application of a Virtual-to-Real Contextual Exercise Rehabilitation Program in Patients with Acute Exacerbation of COPD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120673
Enrollment
Unknown
Registered
2026-03-18
Start date
2025-03-10
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD)

Interventions

Experimental Group:Experimental Group: Based on standardized respiratory rehabilitation and nursing interventions, the group will use virtual reality equipment to simulate virtual walking exercises th
Control Group:No VR training for fear of breathing difficulties, and receive standardized respiratory rehabilitation and nursing intervention

Sponsors

The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The diagnosis meets the criteria for chronic obstructive pulmonary disease. 2. The condition is in the acute exacerbation stage. 3. The Borg score for breathing difficulty during exercise is 3 or above. 4. The score on the breathing difficulty belief questionnaire is above 33. 5. The individual can understand and cooperate with the virtual reality operation and walking test. 6. The participant voluntarily participates in the study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Not meeting the diagnostic criteria for chronic obstructive pulmonary disease; 2. Patients with critical condition and unstable vital signs; 3. Patients with mental disorders; 4. Patients with restricted physical activities; 5. Patients who withdrew from the experiment for various reasons and did not complete the study.

Design outcomes

Primary

MeasureTime frame
6-minute walking distance;Average effective steps;

Secondary

MeasureTime frame
Difficulty in breathing and fear level;Balance test level;Exercise self-efficacy;Degree of breathing difficulty;Lung function;

Countries

China

Contacts

Public ContactHan Yanxia

The First Affiliated Hospital of Soochow University

1249871127@qq.com+86 512 6797 2659

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026