Impact of Pulmonary Rehabilitation After Lung Resection for Cancer on Patients' Level of Anxiety and Depression

• Sponsor: Centre Hospitalier Universitaire de Nice (Other)
• Overall Status: Completed
• CT.gov ID: NCT04985474
• Collaborator: (none)
• Enrollment: 133
• Duration (Months): 23

Study Details

Study Description

Brief 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 .

Condition or Disease	Intervention/Treatment	Phase
Pulmonary Resection	Other: questionnaires

Study Design

• Study Type: Observational
• Actual Enrollment: 133 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Impact of Pulmonary Rehabilitation After Lung Resection for Cancer on Patients' Level of Anxiety and Depression
• Study Start Date: Jan 1, 2011
• Actual Primary Completion Date: Jan 1, 2011
• Actual Study Completion Date: Dec 1, 2012

Arms and Interventions

Arm	Intervention/Treatment
Pulmonary resection	Other: questionnaires

Outcome Measures

Primary Outcome Measures

1. level of depression with scale [At 6 months]

   Assess the level of depression during and after a respiratory rehabilitation training in institutions

2. level of anxiety withe scale [At 6 months]

   Assess the level of anxiety during and after a respiratory rehabilitation training in institutions

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Patient with pulmonary resection

• Patients undergoing a standardized approach (or thoratomie videothoracoscopy)

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• Centre Hospitalier Universitaire de Nice

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Centre Hospitalier Universitaire de Nice
• ClinicalTrials.gov Identifier: NCT04985474
• Other Study ID Numbers: 15-METHODO-02
• First Posted: Aug 2, 2021
• Last Update Posted: Aug 2, 2021
• Last Verified: Jul 1, 2021

• Additional relevant MeSH terms: Depression

Study Results

No Results Posted as of Aug 2, 2021