Quality of Life of Caregivers and Patients Suffering From Multiple System Atrophy

Multiple System Atrophy Clinical Trial

— QUA2-AMS  

Official title:

Quality of Life of Caregivers and Patients Suffering From Multiple System Atrophy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04965922
• Other study ID #: CHUBX 2020/29
• Status: Recruiting
• Phase: N/A
• Start date: July 1, 2021
• Est. completion date: July 1, 2023

Study information

• Verified date: August 2021
• Source: University Hospital, Bordeaux
• Contact: Alexandra FOUBERT-SAMIER
• Phone: 05 57 82 14 20
• Email: alexandra.samier-foubert[@]u-bordeaux.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Multiple system atrophy (MSA) is a rare and fatal neurodegenerative disorder that cause as other neurodegenerative diseases profound declines in functioning and thus, require caregiving for assistance with daily living. The aim of the study is to evaluate the effect of a multimodal intervention as proposed by the NYU Caregiver Counseling and Support Intervention (NYUCI) on the quality of life of patients and their caregivers.

Description:

Multiple system atrophy (MSA) is a rare and fatal neurodegenerative disorder, which is characterized by a variable combination of parkinsonism, cerebellar dysfunction, autonomic failure, and additional signs. No effective treatment is available. MSA patients have a poor prognosis with a median survival ranging between 6 and 10 years. MSA as other neurodegenerative diseases cause profound declines in functioning ; thus, many patients require caregivers for assistance with daily living. Caregiving can also be extremely stressful, and many caregivers experience declines in mental health. All of these repercussions contribute to the deterioration of the caregiver's quality of life and they can have an impact on the patient, in particular, on the patient's survival. Improving quality of life is a major element and identifying effective targeted interventions would bring immediate and direct benefit to patients and their families. In this context, it seems that a multimodal intervention as proposed by the NYU Caregiver Counseling and Support Intervention (NYUCI) developed by Mittelman could contribute to improve disease management and better coping with daily living difficulties. The NYUCI strategy combines sessions of individual and family counseling, support group participation, and additional on-call telephone consultations in a flexible counseling approach that is tailored to each caregiving family

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 144
• Est. completion date: July 1, 2023
• Est. primary completion date: July 1, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Patients Inclusion Criteria :

• Patients suffering from "possible" or "probable" MSA according to clinical consensus criteria
• Living at home
• Presence of at least one close person (family caregiver or not) in the entourage
• Unified Multiple System Atrophy Rating Scale (UMSARS) IV =4
• Written informed consent
• Patient covered by the national health system

Caregivers Inclusion Criteria :

• Age > 18
• Able to answer to study scales and survey
• Written informed consent

Patients Exclusion Criteria:

• Unified Multiple System Atrophy Rating Scale (UMSARS) IV > 4
• Absence of at least one close person

Caregivers Inclusion Criteria :

• Enable to answer to study scales and survey

Related Conditions & MeSH terms

• Atrophy
• Multiple System Atrophy
• Shy-Drager Syndrome

Intervention

Behavioral:
• Multimodal intervention
The intervention consists of identifying the individual needs of each caregiver and patient and identifying sources of improvement in the management of daily life, including the optimization of social support. This optimization requires the involvement of people in the environment (family, friends, neighbours) who can provide help, support of any kind, recurrent or punctual, minimizing negative family interactions and maximizing positive contributions by each in supporting and supporting the individual. The intervention is personalized in the sense that the content of each session seeks to adapt itself to the specificities of the couple situation and its surroundings. interviews/meetings involving a psychologist social worker.

Locations

Country	Name	City	State
France	CHU Bordeaux	Bordeaux

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Multiple System Atrophy Quality of Life (MSA-QoL) Score	Score of emotional and social sub-dimension of the MSA Quality of Life scale. Quality of life questionnaire to collect the level of difficulty experienced by the patient (from no problem to extreme problem) during the 4 weeks preceding the interview on activities such as: moving; walking; maintaining balance; speak; feed oneself. It also assesses the patient's feelings about his illness.	Day 0
Primary	Multiple System Atrophy Quality of Life (MSA-QoL) Score	Score of emotional and social sub-dimension of the MSA Quality of Life scale. Quality of life questionnaire to collect the level of difficulty experienced by the patient (from no problem to extreme problem) during the 4 weeks preceding the interview on activities such as: moving; walking; maintaining balance; speak; feed oneself. It also assesses the patient's feelings about his illness.	6 month
Primary	Multiple System Atrophy Quality of Life (MSA-QoL) Score	Score of emotional and social sub-dimension of the MSA Quality of Life scale. Quality of life questionnaire to collect the level of difficulty experienced by the patient (from no problem to extreme problem) during the 4 weeks preceding the interview on activities such as: moving; walking; maintaining balance; speak; feed oneself. It also assesses the patient's feelings about his illness.	12 month
Secondary	Center for Epidemiologic Sutdies-Depression (CESD) Score	20 items scale used to assess the existence of a depressive syndrome. Scores less than 15 does not indicate any depressive disorder Scores between 15 and 21 are indicative of mild to moderate depression. Scores above 21 are consistent with the existence of severe/ major depression	Day 0
Secondary	Center for Epidemiologic Sutdies-Depression (CESD) Score	20 items scale used to assess the existence of a depressive syndrome. Scores less than 15 does not indicate any depressive disorder Scores between 15 and 21 are indicative of mild to moderate depression. Scores above 21 are consistent with the existence of severe/ major depression	3 month
Secondary	Center for Epidemiologic Sutdies-Depression (CESD) Score	20 items scale used to assess the existence of a depressive syndrome. Scores less than 15 does not indicate any depressive disorder Scores between 15 and 21 are indicative of mild to moderate depression. Scores above 21 are consistent with the existence of severe/ major depression	6 month
Secondary	Multiple System Atrophy Quality of Life (MSA-QoL) Score	Score of other sub-dimension of the MSA Quality of Life scale. The MSA-QoL questionnaire is composed of three different subscales: motor (14 items), non-motor (12 items) and emotional/social (14 items). The response options for each question range from 0 (no problem) to 4 (extreme problem) with higher total scores reflecting more impaired quality of life. The MSA-QoL also includes a visual analogue scale (VAS) of how satisfied patients feel (range 0-100, with lower scores indicating lower quality of life).	Day 0
Secondary	Multiple System Atrophy Quality of Life (MSA-QoL) Score	Score of other sub-dimension of the MSA Quality of Life scale. The MSA-QoL questionnaire is composed of three different subscales: motor (14 items), non-motor (12 items) and emotional/social (14 items). The response options for each question range from 0 (no problem) to 4 (extreme problem) with higher total scores reflecting more impaired quality of life. The MSA-QoL also includes a visual analogue scale (VAS) of how satisfied patients feel (range 0-100, with lower scores indicating lower quality of life).	3 month
Secondary	Multiple System Atrophy Quality of Life (MSA-QoL) Score	Score of other sub-dimension of the MSA Quality of Life scale. The MSA-QoL questionnaire is composed of three different subscales: motor (14 items), non-motor (12 items) and emotional/social (14 items). The response options for each question range from 0 (no problem) to 4 (extreme problem) with higher total scores reflecting more impaired quality of life. The MSA-QoL also includes a visual analogue scale (VAS) of how satisfied patients feel (range 0-100, with lower scores indicating lower quality of life).	6 month
Secondary	State Trait Inventory Anxiety (STAI) Score	Anxiety assessment. 2 scales of 20 questions used to assess how subjects feel at the time and generally. Score > 65 means high anxiety ; Score < 35 means low anxiety	Day 0
Secondary	State Trait Inventory Anxiety (STAI) Score	Anxiety assessment. 2 scales of 20 questions used to assess how subjects feel at the time and generally. Score > 65 means high anxiety ; Score < 35 means low anxiety	3 month
Secondary	State Trait Inventory Anxiety (STAI) Score	Anxiety assessment. 2 scales of 20 questions used to assess how subjects feel at the time and generally. Score > 65 means high anxiety ; Score < 35 means low anxiety	6 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) I	(0=no disorder, 48=severe disorders): Is an assessment of daily life activities via 12 12 items scale used to assess language, writing, autonomy , walking and the presence of possible urinary, sexual or intestinal disorders. (0=no disorder, 48=severe)	Day 0
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) I	(0=no disorder, 48=severe disorders): Is an assessment of daily life activities via 12 12 items scale used to assess language, writing, autonomy , walking and the presence of possible urinary, sexual or intestinal disorders. (0=no disorder, 48=severe)	3 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) I	(0=no disorder, 48=severe disorders): Is an assessment of daily life activities via 12 12 items scale used to assess language, writing, autonomy , walking and the presence of possible urinary, sexual or intestinal disorders. (0=no disorder, 48=severe)	6 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) II	Motor examination based on 14 items that allow to evaluate in particular facial expression, oculomotricity, oral expression, tremors or walking. 0=no disorder, 56=severe disorders	Day 0
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) II	Motor examination based on 14 items that allow to evaluate in particular facial expression, oculomotricity, oral expression, tremors or walking. 0=no disorder, 56=severe disorders	3 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) II	Motor examination based on 14 items that allow to evaluate in particular facial expression, oculomotricity, oral expression, tremors or walking. 0=no disorder, 56=severe disorders	6 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) III	Blood pressure and heart rate measurements in the lying and standing position for 10 min every minute.	Day 0
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) III	Blood pressure and heart rate measurements in the lying and standing position for 10 min every minute.	3 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) III	Blood pressure and heart rate measurements in the lying and standing position for 10 min every minute.	6 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) IV	Assessment of the disability from 1 to 5. 1 = completely independent ; 5 = totally dependent	Day 0
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) IV	Assessment of the disability from 1 to 5. 1 = completely independent ; 5 = totally dependent	3 month
Secondary	Unified Multiple System Atrophy Rating Scale (UMSARS) IV	Assessment of the disability from 1 to 5. 1 = completely independent ; 5 = totally dependent	6 month
Secondary	Montreal Cognitive Assessment (MoCA) Score	evaluates short-term memory, visuospatial skills, executive functions, attention, concentration, work memory, language, abstraction, computation, and time and space orientation. Cognitive impairment is assessed by the score on 30 points (27-30: no cognitive impairment; 21-26: mild).	Day 0
Secondary	Montreal Cognitive Assessment (MoCA) Score	evaluates short-term memory, visuospatial skills, executive functions, attention, concentration, work memory, language, abstraction, computation, and time and space orientation. Cognitive impairment is assessed by the score on 30 points (27-30: no cognitive impairment; 21-26: mild).	3 month
Secondary	Montreal Cognitive Assessment (MoCA) Score	evaluates short-term memory, visuospatial skills, executive functions, attention, concentration, work memory, language, abstraction, computation, and time and space orientation. Cognitive impairment is assessed by the score on 30 points (27-30: no cognitive impairment; 21-26: mild).	6 month
Secondary	Zarit Scale score	Assesses caregiver burden. 22 item scale with total score ranging from 0 to 88. Score 20 mean zero load - Score > 60 means severe load	Day 0
Secondary	Zarit Scale score	Assesses caregiver burden. 22 item scale with total score ranging from 0 to 88. Score 20 mean zero load - Score > 60 means severe load	3 month
Secondary	Zarit Scale score	Assesses caregiver burden. 22 item scale with total score ranging from 0 to 88. Score 20 mean zero load - Score > 60 means severe load	6 month
Secondary	Family Relations Index (FRI)	27 items used to assess family functioning : family cohesion, verbalization of feelings and family conflict.	Day 0
Secondary	Family Relations Index (FRI)	27 items used to assess family functioning : family cohesion, verbalization of feelings and family conflict.	3 month
Secondary	Family Relations Index (FRI)	27 items used to assess family functioning : family cohesion, verbalization of feelings and family conflict.	6 month