Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06652204
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
None
First Post:
2024-10-15
Brief Title:
Validation of the French Version of the QASCI in Caregivers of Patients With COPD
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Validation of the French Version of the Informal Caregiver Burden Assessment Questionnaire QASCI in Caregivers of Patients With COPD VALQASCI
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
VALQASCI
Brief Summary:
This study aims to validate the French version of the QASCI questionnaire initially written and validated in Portuguese language by Hipolito et al to assess caregiving burden in chronic obstructive pulmonary disease COPD
The realization of this validation is significant on several levels First since COPD is a systemic condition it affects not only the lungs but also many other organs and systems in the body It leads to various complications that go beyond respiratory symptoms creating major challenges not only physically but also in terms of participation and involvement for patients and their caregivers The lack of validated tools in French to specifically assess the quality of life of caregivers in this context represents a gap that this study seeks to fill
This study is also justified by the fact that although the QASCI has been validated in other languages and contexts it is essential to linguistically and culturally adapt this tool for the French-speaking population Validation in French is crucial to ensure the fidelity of the results obtained and the validity of the conclusions drawn from this instrument for caregivers of patients with COPD in France
In summary this study addresses a specific need by contributing to the prevention of pathologies among caregivers It enhances early detection and support for caregivers of patients with COPD while paving the way for future research on this often-overlooked population
The realization of this validation is significant on several levels First since COPD is a systemic condition it affects not only the lungs but also many other organs and systems in the body It leads to various complications that go beyond respiratory symptoms creating major challenges not only physically but also in terms of participation and involvement for patients and their caregivers The lack of validated tools in French to specifically assess the quality of life of caregivers in this context represents a gap that this study seeks to fill
This study is also justified by the fact that although the QASCI has been validated in other languages and contexts it is essential to linguistically and culturally adapt this tool for the French-speaking population Validation in French is crucial to ensure the fidelity of the results obtained and the validity of the conclusions drawn from this instrument for caregivers of patients with COPD in France
In summary this study addresses a specific need by contributing to the prevention of pathologies among caregivers It enhances early detection and support for caregivers of patients with COPD while paving the way for future research on this often-overlooked population
Detailed Description:
Beyond its respiratory component COPD being a systemic condition leads to significant problems in various domains for patients Dyspnea remains their main complaint but these patients also experience impairments in physical capacity nutritional status and symptoms of anxiety and depression which can limit their daily physical activity and reduce their quality of life even their life expectancy
As the disease progresses patients become increasingly dependent on care experiencing difficulties in performing activities of daily living ADLs and social isolation is often observed
In this context caregivers usually a spouse or child play a crucial role in supporting patients with ADLs providing assistance with medical care and symptom management Their presence is essential for facilitating and improving patients adherence to COPD management behaviors such as treatment compliance or increasing daily physical activity Thus their role in the healthcare system is fundamental both as a link to medical teams and as support for the patient
However assuming the caregiver role can heavily impact the caregivers physical psychological and social well-being A survey in Spain reveals that many caregivers face health issues and experience reduced social leisure and professional activities due to their role Additionally they may feel helpless anxious depressed and vulnerable to fatigue incapacity andor burnout while trying to cope with the demands related to COPD Other studies highlight the professional impact of caregiver status with absences linked to this situation or decreased work effectiveness This situation can be even more challenging for caregivers of patients with advanced COPD who face higher risks of exacerbations hospitalizations and mortality compared to less severely affected patients
It is therefore essential that healthcare professionals and paramedical staff who work with COPD patients and their caregivers have a tool to assess the burden on informal caregivers To date the only existing tool seems to be the QASCI questionnaire drafted and validated in Portuguese by Hipólito et al However due to the language barrier this tool cannot be used with French-speaking populations
It is in this context that the present study finds its place with the aim of establishing the validity and reliability of the French translation of the QASCI questionnaire
As the disease progresses patients become increasingly dependent on care experiencing difficulties in performing activities of daily living ADLs and social isolation is often observed
In this context caregivers usually a spouse or child play a crucial role in supporting patients with ADLs providing assistance with medical care and symptom management Their presence is essential for facilitating and improving patients adherence to COPD management behaviors such as treatment compliance or increasing daily physical activity Thus their role in the healthcare system is fundamental both as a link to medical teams and as support for the patient
However assuming the caregiver role can heavily impact the caregivers physical psychological and social well-being A survey in Spain reveals that many caregivers face health issues and experience reduced social leisure and professional activities due to their role Additionally they may feel helpless anxious depressed and vulnerable to fatigue incapacity andor burnout while trying to cope with the demands related to COPD Other studies highlight the professional impact of caregiver status with absences linked to this situation or decreased work effectiveness This situation can be even more challenging for caregivers of patients with advanced COPD who face higher risks of exacerbations hospitalizations and mortality compared to less severely affected patients
It is therefore essential that healthcare professionals and paramedical staff who work with COPD patients and their caregivers have a tool to assess the burden on informal caregivers To date the only existing tool seems to be the QASCI questionnaire drafted and validated in Portuguese by Hipólito et al However due to the language barrier this tool cannot be used with French-speaking populations
It is in this context that the present study finds its place with the aim of establishing the validity and reliability of the French translation of the QASCI questionnaire
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None