Investigation on the Current Situation of Fear of Exercise in Patients with Stable COPD

A cross-sectional study on kinesiophobia in patients with stable chronic obstructive pulmonary disease

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2600121705

Enrollment

Unknown

Registered

2026-04-01

Start date

2026-04-01

Completion date

Unknown

Last updated

2026-04-14

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

Conditions

Exercise fear in patients with chronic obstructive pulmonary disease (COPD) during the stable phase

Interventions

Observation group:None

Eligibility

Sex/Gender

All

Age

55 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Meets the clinical diagnostic criteria for chronic obstructive pulmonary disease (COPD) and is in a stable phase of the disease. 2.No restrictions on age or gender, covering different stages of disease progression (short, medium, and long-term). 3.Patients at any GOLD stage are eligible, with or without a history of acute exacerbations. 4.Able to understand the content of the assessment scale, or complete the questionnaire with assistance (individuals with cognitive impairment may complete it through interview-style assistance); 5.Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Individuals with severe organic diseases such as serious cardiovascular and cerebrovascular diseases, liver or kidney failure, or malignant tumors who are unable to cooperate with the assessment process; 2.Individuals with severe mental disorders or significant cognitive impairment who are unable to communicate effectively or comprehend the assessment process; 3.Individuals who have experienced an acute exacerbation of COPD within the past three months, or who are currently experiencing an acute flare-up of another disease; 4.Individuals unable to perform basic physical activities due to physical functional impairments (such as severe arthritis, hemiplegia, etc.), affecting movement-related assessments; 5.Individuals who refuse to participate in the study or are unable to cooperate throughout the entire evaluation process.

Design outcomes

Primary

Measure	Time frame
Level of Exercise Aversion;	—

Secondary

Measure	Time frame
Disease-related characteristics;	—

Countries

China

Contacts

Public ContactWang Tong

Shanghai Second Rehabilitation Hospital

wt19535903056@163.com+86 21 66181108

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026