Status and Develepment Mental Quality of Life COPD/IPF Inpatients Before and After Pulmonary Rehabilitation

Sponsor

Schön Klinik Berchtesgadener Land (Other)

Overall Status

Terminated

CT.gov ID

NCT03477526

Collaborator

Lungenfibrose e.V. (Other)

Enrollment

Location

Arms

Actual Duration (Days)

30.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

As the result of our last study "Long Term effects of an Inpatient Pulmonary Program in Patients with Pulmonary Fibrosis" already demonstrated the positive effects of a Pulmonary Rehabiliation on the mental status. In this current study the aim will be to analyse the personality type regarding anxiety and depression

Condition or Disease	Intervention/Treatment	Phase
Idiopathic Pulmonary Fibrosis and COPD	Procedure: Pulmonary rehabilitation program	N/A

Study Design

Study Type:

Interventional

Actual Enrollment :

1 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Health Services Research

Official Title:

Status and Develepment Mental Quality of Life in Lung Fibrosis in Comparison of COPD Inpatients Before and After Pulmonary Rehabilitation

Actual Study Start Date :

Feb 26, 2019

Actual Primary Completion Date :

Feb 27, 2019

Actual Study Completion Date :

Feb 27, 2019

Arms and Interventions

Arm	Intervention/Treatment
Experimental: COPD patients (GOLD stage III-IV)	Procedure: Pulmonary rehabilitation program 3 weeks, ...
Active Comparator: IPF patients	Procedure: Pulmonary rehabilitation program 3 weeks, ...

Arm

Intervention/Treatment

Experimental: COPD patients (GOLD stage III-IV)

Procedure: Pulmonary rehabilitation program

3 weeks, ...

Active Comparator: IPF patients

Procedure: Pulmonary rehabilitation program

3 weeks, ...

Outcome Measures

Primary Outcome Measures

Anxiety score [3 weeks]
Hospital Anxiety and Depression scale

Secondary Outcome Measures

Anxiety score [3 months]
Hospital Anxiety and Depression scale

Eligibility Criteria

Criteria

Ages Eligible for Study:

50 Years to 80 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

COPD GOLD III-IV
IPF according Pulmonary Guidelines

Exclusion Criteria:

< 30% FVC comorbidities with a negativ influence on the prognosis neurological and orthopaedic deficits, which make the participation of the pulmonary rehabilitation impossible non-compliance no written informed consent of the patient