About this trial
The goal of this clinical trial is two-fold. First to investigate the feasibility of whether a remotely administered smartphone app can increase the volume and intensity of physical activity in daily life in individuals with a LRRK2 G2019S or GBA1 N370S genetic mutation over a long period of time (24 months). Second, to explore the preliminary efficacy of exercise on markers for prodromal Parkinson's disease progression in individuals with a LRRK2 G2019S or GBA1 N370S genetic mutation.
Participants will be tasked to achieve an incremental increase of daily steps (volume) and amount of minutes exercised at a certain heart rate (intensity) with respect to their own baseline level. Motivation with regards to physical activity will entirely be communicated through the study specific Slow Speed smartphone app. A joint primary objective consists of two components. First to determine the longitudinal effect of an exercise intervention in LRRK2 G2019S or GBA1 N370S variant carriers on a prodromal load score, comprised of digital biomarkers of prodromal symptoms. The secondary component of the primary outcome is to determine the feasibility of a remote intervention study. The secondary objective is the effect of a physical activity intervention on digital markers of physical fitness. Exploratory outcomes entail retention rate, completeness of remote digital biomarker assessments, digital prodromal motor and non-motor features of PD. Using these biomarkers, the investigators aim to develop a composite score (prodromal load score) to estimate the total prodromal load. An international exercise study with fellow researchers in the United Kingdom are currently in preparation (Slow-SPEED-UK) and active in the Netherlands (Slow-SPEED-NL). Our intention is to analyse overlapping outcomes combined where possible through a meta-analysis plan, to obtain insight on (determinants of) heterogeneity in compliance and possible efficacy across subgroups
Eligibility criteria
Qualifiers
previously identified LRRK2 G2019S or GBA N370S variant based on genotyping
aged 50 years or older
able to understand the English language
being able to walk independently inside the home without the use of a walking aid
Disqualifiers
clinically diagnosed or self-reported diagnosis neurodegenerative disease
self-reported falls of three or more per year
dexterity problems or cognitive impairments hampering smartphone use
if they are not aware of and do not wish to be informed about an increased risk of developing diseases associated with the LRRK2 or GBA1 risk variant
Trial design
Treatments tested in this trial
- Increase of physical activity volume and intensity with the use of a motivational smartphone application
Treatment groups
Locations
2Sponsors and collaborators
Radboud University Medical Center
Lead sponsor
Stichting ParkinsonNL
Collaborator
ZonMw: The Netherlands Organisation for Health Research and Development
Collaborator
Michael J. Fox Foundation for Parkinson's Research
Collaborator
Parkinson's UK
Collaborator
Cure Parkinson's
Collaborator
Edmond J. Safra Foundation
Collaborator
Davis Phinney Foundation
Collaborator
Sleep Medicine Centre Kempenhaeghe
Collaborator
Sleep Medicine Centre SEIN
Collaborator
Queen Mary University of London
Collaborator
23andMe, Inc.
Collaborator
Parkinsons Progression Markers Initiative (PPMI)
Collaborator
Massachusetts General Hospital
Collaborator
Harvard School of Public Health (HSPH)
Collaborator
IJsfontein B.V., Netherlands
Collaborator
Hoffmann-La Roche
Collaborator
Erasmus Medical Center
Collaborator
University of Illinois at Chicago
Collaborator
University of Rochester
Collaborator
University of Bristol
Collaborator
University of Plymouth
Collaborator
University of Luebeck
Collaborator
McGill University
Collaborator
University of Pittsburgh
Collaborator
Donders Centre for Cognitive Neuroimaging
Collaborator
Parkinson's Foundation
Collaborator