Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT03638505

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Screening

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Trial Site Locations

Total: 1 location

1

Assistance Publique Des Hopitaux de Marseille

Marseille, PACA, France, 13354

Actively Recruiting

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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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