Effect on Quality of Life of Adapted Information in Pulmonary Rehabilitation in Chronic Respiratory Disease Patients

Chronic Respiratory Disease Clinical Trial

Official title:

Effect on Quality of Life of Information Aimed at Reducing the Impact of a Personality Trait (Openness to Experiences) Identified as a Risk of Non-response to Pulmonary Rehabilitation in Patients With Chronic Respiratory Diseases

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05325086
• Other study ID #: MONTREHAL-1
• Status: Completed
• Phase: N/A
• Start date: April 5, 2022
• Est. completion date: July 25, 2023

Study information

• Verified date: July 2023
• Source: Korian
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the clinical study is to study the effect of health-related quality of Life of information aimed at reducing the impact of a personality trait (openness to experiences) identified as a risk of non-response to pulmonary rehabilitation in patients with chronic respiratory diseases. This study will determine if a specific information focusing on characteristics of openness to experiences personality trait will lead to better benefits than a general information.

Description:

According to the Five Factor Model, personality is made of five dimensions present in varying degrees in individuals and influencing their behavior and life experiences. Several studies showed that some personality traits, according to their level, may positively or negatively influence the quality of life. They can also have an impact on the benefits obtained at the end of one treatment. In the particular context of pulmonary rehabilitation (PR) which is one of the most efficient treatment in respiratory diseases, it has been showed that with a classical support, higher scores for openness to experiences represent a risk factor for non-response in PR on quality of life (i.e. no improvement). Several authors showed that adapted interventions (ex: simple information booklets), based on personality traits, can enhance the effectiveness of the intervention. Considering that in chronic respiratory diseases, openness to experiences when it is more marked represents a risk of not improving the quality of life following a PR program, the idea of offering information in line with the characteristics of these people (i.e., search for novelties, autonomy, broad and varied interests, etc.) seems relevant and feasible. The investigators hypothesize that the patients receiving an adapted information aimed at reducing the impact of a personality trait (openness to experiences) will better improve their quality of life in comparison with the patients receiving a neutra information. The main objective is to assess the impact of life of an adapted information during pulmonary rehabilitation on quality in patients with chronic respiratory diseases.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 136
• Est. completion date: July 25, 2023
• Est. primary completion date: July 25, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

Admitted for a 4-week inpatient pulmonary rehabilitation program Chronic respiratory disease diagnosis 18 and 80 years old Reading and writing skills Oral consent Exclusion Criteria: Inability to participate to exercise training Inability to answer a questionnaire Severe or unstable heart disease, orthopedic, neurologic or psychiatric comorbidities Recent exacerbation (<4 weeks) Pregnant and breastfeeding women Protected adults, pregnant women Participation in another study, with the exception of observational studies

Related Conditions & MeSH terms

• Chronic Respiratory Disease
• Respiration Disorders
• Respiratory Tract Diseases

Intervention

Other:
• Adapted information arm
A adapted booklet will be delivered to patients at the start of the stay. This booklet contains adapted information about the pulmonary rehabilitation targetting the characteristics of the openness to experiences personality traits
• Neutral information arm
A neutral booklet will be delivered to patients at the start of the stay. This booklet contains neutral information about the pulmonary rehabilitation

Locations

Country	Name	City	State
France	Clinique du Souffle le Pontet	Hauteville-Lompnes
France	Clinique du Souffle Les Clarines	Riom-ès-Montagnes

Sponsors (1)

Lead Sponsor	Collaborator
Korian

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Differential of health-related quality of life from baseline to PR end-stay	Assessing differential of health-related quality of life score on St. George's Respiratory Questionnaire (SGRQ) (Jones et al., 1991) from baseline to PR end-stay within and between groups; The SGRQ contains 50 questions and evaluates 3 dimensions : symptoms component, activities that cause or are limited by breathlessness and impact component	Changes from baseline (T0) to at the end of the 4-weeks PR (T1)
Secondary	Differential of dyspnea from from baseline to PR end-stay	Assessing differential of dyspnea score on DYSPNEA-12 questionnaire (Yorke et al 2010) within and between groups.; The Dyspnea-12 contains 12items and evaluate the physical and affective dimensions of dyspnea.	Changes from baseline (T0) to at the end of the 4-weeks PR (T1)
Secondary	Differential of exercise tolerance from from baseline to PR end-stay	Assessing differential of exercise tolerance on the 6-minute walking test within and between groups.	Changes from baseline (T0) to at the end of the 4-weeks PR (T1)
Secondary	Differential of self-efficacy from from baseline to PR end-stay	Assessing differential of self-efficacy score on Self-efficacy for managing chronic disease SEMCD-6 questionnaire (Ritter & Lorig, 2014) within and between groups. This questionnaire contains 6 items.	Changes from baseline (T0) to at the end of the 4-weeks PR (T1)
Secondary	Differential of disease-related thinking from from baseline to PR end-stay	Assessing differential of disease-related thinking score on Brief Illness Perception Questionnaire B-IPQ (Broadbent et al., 2006) within and between groups.; This questionnaire contains 8 items.	Changes from baseline (T0) to at the end of the 4-weeks PR (T1)
Secondary	Differential of disease-related fears from from baseline to PR end-stay	Assessing differential of disease-related fears score on COPD Anxiety Questionnaire Revised CAF-R (Keil et al., 2014) within and between groups.; This questionnaire contains 20 items.	Changes from baseline (T0) to at the end of the 4-weeks PR (T1)