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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04985474
Other study ID # 15-METHODO-02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2011
Est. completion date December 2012

Study information

Verified date July 2021
Source Centre Hospitalier Universitaire de Nice
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The interest of pulmonary rehabilitation for patients who underwent lung resection for cancer remains controversial. The investigators studied the effects of the RR and its impact on quality of life and level of anxiety and depression in patients. In 2011 and 2012 , an RR was proposed to the patients referred to our center after lung resection for cancer. Patients were assessed at entry and departure by 6minutes walk test , a visual analog pain scale , a quality of life questionnaire ( EORTC QLQ C30 ) and an anxiety questionnaire and Depression (HAD) . These same questionnaires were mailed 6 months after the end of the pulmonary rehabilitation .


Recruitment information / eligibility

Status Completed
Enrollment 133
Est. completion date December 2012
Est. primary completion date January 2011
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patient with pulmonary resection - Patients undergoing a standardized approach (or thoratomie videothoracoscopy)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
questionnaires


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Outcome

Type Measure Description Time frame Safety issue
Primary level of depression with scale Assess the level of depression during and after a respiratory rehabilitation training in institutions At 6 months
Primary level of anxiety withe scale Assess the level of anxiety during and after a respiratory rehabilitation training in institutions At 6 months
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