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COhort of patients with PArkinson's DIsease in Spain, 2015 (COPPADIS-2015)
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Sample details

COPPADIS-2015 aimed to assess the progression and impact of Parkinson's Disease (PD) in Spain. Beginning in 2015, the study involved over 1,100 individuals, of which 694 were PD patients, 273 were caregivers, and 207 were control participants. These individuals were recruited between 2016 and 2017, and participants with PD ranged from 30 to 75 years old. Participants were followed up annually for 5 years, with the follow-up concluded at the end of 2023.

Study design
Cohort - clinical

Number of participants at first data collection

694 (participants with Parkinson's disease)

207 (controls)

273 (caregivers of participants with Parkinson's disease)

Age at first data collection

30 - 75 years (participants with Parkinson's disease)

Varied (controls)

Varied (caregivers of participants with Parkinson's disease)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adults
Caregivers
Older and elderly people
People with mild and major neurocognitive disorders
Dataset details

Country

Spain

Year of first data collection

2015

Primary Institutions

Moisés Broggi Hospital (Hospital Moisés Broggi)

Alcorcón Hospital Foundation (Fundación Hospital de Alcorcón)

Architect Marcide Hospital (Arquitecto Marcide Hospital)

Arnau de Vilanova Hospital (Hospital Arnau de Vilanova)

Burgos University Hospital Complex (Complejo Asistencial Universitario de Burgos)

Links

doi.org/10.1111/ene.14008

Funders

Acebre

Valencia Parkinson's Association (Asociación Parkinson Valencia)

AbbVie

City Council of Coruña (Ayuntamiento de A Coruña)

Climanosa

Ongoing?
No

Data types collected

neuroImagingData
mentalHealthData
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Self-report questionnaire – unspecified
Qualitative data collection
  • None
Neuroimaging data collection
  • Magnetic Resonance Imaging (MRI)
Linked or secondary data
  • None
Features

Engagement

  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Caregiving
    Cognitive ageing and decline
    Disease progression
    Longstanding illness and disability
    Motor difficulties
    Parkinson's disease (PD)
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