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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04965922
Acronym
QUA2-AMS
Enrollment
130
Registered
2021-07-16
Start date
2021-07-01
Completion date
2025-07-17
Last updated
2026-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple System Atrophy

Keywords

Multiple System Atrophy, Quality of life, Multimodal intervention, Neurodegenerative disease

Brief 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.

Detailed 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

Interventions

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.

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Multiple System Atrophy Quality of Life (MSA-QoL) ScoreDay 0Score 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.

Secondary

MeasureTime frameDescription
Center for Epidemiologic Sutdies-Depression (CESD) ScoreDay 020 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
Multiple System Atrophy Quality of Life (MSA-QoL) ScoreDay 0Score 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).
State Trait Inventory Anxiety (STAI) ScoreDay 0Anxiety 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
Unified Multiple System Atrophy Rating Scale (UMSARS) IDay 0(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)
Unified Multiple System Atrophy Rating Scale (UMSARS) IIDay 0Motor 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
Unified Multiple System Atrophy Rating Scale (UMSARS) IIIDay 0Blood pressure and heart rate measurements in the lying and standing position for 10 min every minute.
Unified Multiple System Atrophy Rating Scale (UMSARS) IVDay 0Assessment of the disability from 1 to 5. 1 = completely independent ; 5 = totally dependent
Montreal Cognitive Assessment (MoCA) ScoreDay 0evaluates 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).
Zarit Scale scoreDay 0Assesses caregiver burden. 22 item scale with total score ranging from 0 to 88. Score 20 mean zero load - Score \> 60 means severe load
Family Relations Index (FRI)Day 027 items used to assess family functioning : family cohesion, verbalization of feelings and family conflict.

Countries

France

Contacts

PRINCIPAL_INVESTIGATORAlexandra FOUBERT-SAMIER

University Hospital, Bordeaux

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 21, 2026