Actively Recruiting
Quality of Life of the Patient and the Burden of the Caregiver in Progressive Supranuclear Palsy
Led by Assistance Publique Hopitaux De Marseille · Updated on 2024-01-08
200
Participants Needed
1
Research Sites
364 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Progressive supranuclear palsy (PSP) is a rare neurodegenerative disease from the parkinsonian syndrome group. PSP is characterised by the association of a non-doparesponsive parkinsonian syndrome with axial signs. The latter predominantly manifest as a psycho-motor slowness, an apathy and frontal executive deficits. Swallowing impairments may additionally provoke life-threatening situations. Today the treatment is mostly symptomatic as no cure is available. Given the limited treatment options and its clinical characteristics, PSP deeply impact on the patients' quality of life (QoL) as well as on their caregivers'. Nevertheless a limited number of studies have focused on these aspects. A better understaning of the factors determining both patient and cargiver QoL may help optimising their care. the principal objective of this study is to identify the determinants of PSP patients' QoL. The secondary objectives are : i) to identify the determinants (medical, behavioural, socio-economic, environmental …) of PSP patients' caregivers' QoL and burden ; ii) to validate in French language the QoL scale specific for PSP available in English (PSP-QoL). This is a multidisciplinary transversal study. 2 subject groups will be included : i) PSP patients ; ii) caregiver of PSP patients (designated by the patient as being the person closest to them), Data collected : i) from the patient : socio-demographic, social and professionnal environment, clinical (disease duration and severity, neuropsychological evaluation), therapeutic, mood, anxiety, coping, body image, QoL ; ii) from the caregiver: socio-demographic, social and professionnal environment, connection with the patient, data relative to their own health, mood, anxiety, coping, QoL, burden. Progress : patient information, designation of a caregiver, consent collection, collection of data Statistical analysis : To address the principal objective 'patient' QoL scores will be confronted to the other collected variables (Student's t-test, correlation coefficient). The results will be adjusted to the confounding factors using multivariate analyses.
CONDITIONS
Official Title
Quality of Life of the Patient and the Burden of the Caregiver in Progressive Supranuclear Palsy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients of either gender aged 40 years or older at symptom onset
- Diagnosis of possible or probable PSP according to Litvan criteria (1996b)
- Agreement to participate in the study
- No severe cognitive impairment (Mini-Mental State score above 20/30)
- No severe psycho-behavioral comorbidity that prevents assessment
- No legal protection measures affecting the patient
- Caregivers aged 18 years or older
- Caregivers designated by the patient as the closest person
- Caregivers agreeing to participate
- Caregivers affiliated to a social security scheme
You will not qualify if you...
- Patients younger than 40 years at symptom onset
- Diagnosis other than PSP, including other Parkinsonian syndromes
- Presence of another neurological disease
- Severe cognitive impairment (Mini-Mental State score 20 or below)
- Severe psycho-behavioral comorbidities preventing evaluation
- Patients under legal protection
- Patients not affiliated to a social security scheme
- Caregivers younger than 18 years
- Caregivers not designated by the patient as the closest person
- Caregivers not agreeing to participate
- Caregivers not affiliated to a social security scheme
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Trial Site Locations
Total: 1 location
1
Assistance Publique Des Hopitaux de Marseille
Marseille, PACA, France, 13354
Actively Recruiting
Research Team
A
ALEXANDRE EUSEBIO, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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