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Construction and application of an intervention program for patients with interstitial lung disease based on Monitor and Acceptance Theory

Construction and application of an intervention program for patients with interstitial lung disease based on Monitor and Acceptance Theory

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073118
Enrollment
Unknown
Registered
2023-07-03
Start date
2023-05-01
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Interstitial lung disease

Interventions

Control Group:Treatment as usual.
Intervention Group 1:Pulmonary rehabilitation training.
Intervention Group 2:Pulmonary rehabilitation training based on Monitor and Acceptance Theory.
Cross-sectional survey:None.

Sponsors

The Second Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for cross-sectional study: Patients diagnosed with interstitial lung disease by PCCM specialist physicians; aged 18 or older; informed consent and voluntary participation in this survey. 2. Inclusion criteria for quasi-experimental study: Adult patients diagnosed with interstitial lung disease by PCCM specialist physicians; those who meet the pulmonary rehabilitation indications in the "Guidelines for respiratory rehabilitation management of chronic respiratory diseases in China"; Montreal Cognitive Assessment (MoCA) score < 26; informed consent and voluntary participation in this research.

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for cross-sectional studies: individuals in acute stage of disease or with severe respiratory distress unable to cooperate with the investigation; individuals lacking language proficiency to independently complete the assessment scales; individuals with severe visual or hearing impairments. 2. Exclusion criteria for quasi-experimental studies: individuals currently participating in intervention programs similar to this study; individuals unable to correctly complete the specified tasks; individuals with functional or organic mental disorders; individuals taking antipsychotic medications; individuals experiencing sudden changes in condition during the intervention that affect cognitive function.

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Secondary

MeasureTime frame
Mindfulness level;Anxiety, Depression;Dyspnea degree;Pulmonary function;Quality of life;Pulmonary rehabilitation adherence;

Countries

China

Contacts

Public ContactDanhua Qu

The Second Hospital of Jilin University

qudh@jlu.edu.cn+86 159 0443 7721

Outcome results

None listed

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