NCT03130595

Brief Summary

WestPORTS will recruit a randomly selected population consisting of 25% of all individuals with Parkinson's disease (ICD G209) that have visited any of the seven major outpatient neurology or geriatrics clinics in West Sweden (population 1.7M) during a predefined 12 month period between Sept 2016 and April 2018. Baseline clinical and demographic data will be collected along with a 6 x 24h accelerometry recording using the Parkinson Kinetigraph (Global Kinetics). Repeated data collections will be made with regular intervals of up to 2 years as long as subjects are alive and willing.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
320

participants targeted

Target at P75+ for all trials

Timeline
56mo left

Started Apr 2017

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress66%
Apr 2017Dec 2030

First Submitted

Initial submission to the registry

April 22, 2017

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 26, 2017

Completed
Same day until next milestone

Study Start

First participant enrolled

April 26, 2017

Completed
8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
5.6 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2030

Expected
Last Updated

November 27, 2024

Status Verified

November 1, 2024

Enrollment Period

8 years

First QC Date

April 22, 2017

Last Update Submit

November 26, 2024

Conditions

Keywords

accelerometryParkinson Kinetigraph

Outcome Measures

Primary Outcomes (1)

  • Objective measurement of spontaneous movement patterns

    Parkinson Kinetigraph

    144 hours

Study Arms (1)

PD outpatients in West Sweden

Cross-sectional random sample of patients with PD that have visited outpatient clinics in West Sweden in the last 6+6 months

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

25% of the population described by the inclusion criteria

You may qualify if:

  • Medical record with a G209 (Parkinson's disease) diagnosis
  • A visit to one of the participating outpatient clinics in West Sweden within the last 6 months
  • Informed consent

You may not qualify if:

  • Diagnosis revised before visit.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sahlgrenska University Hospital

Gothenburg, 41345, Sweden

Location

MeSH Terms

Conditions

Parkinson DiseaseParkinsonian Disorders

Condition Hierarchy (Ancestors)

Basal Ganglia DiseasesBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesMovement DisordersSynucleinopathiesNeurodegenerative Diseases

Study Officials

  • Filip Bergquist, MD, PhD

    Göteborg University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
PROSPECTIVE
Target Duration
15 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

April 22, 2017

First Posted

April 26, 2017

Study Start

April 26, 2017

Primary Completion

May 1, 2025

Study Completion (Estimated)

December 1, 2030

Last Updated

November 27, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will share

Clinical registry data will be immediately available as part of the national Parkinson Registry. Study specific data from objective measurements will be made available within the registry one year after final subject has been recruited. Access to data requires ethical permission and permission from the registry scientific committee SWEPAR.

Shared Documents
STUDY PROTOCOL
Time Frame
See plan description
Access Criteria
Access to data requires ethical permission and permission from the registry scientific committee SWEPAR.
More information

Locations