About this trial
The goal of this clinical trial (feasibility study) is to learn if a multimodal lifestyle program can improve adherence to recommended lifestyle changes in people with REM Sleep Behavior Disroder (RBD) or Parkinson's disease (PD).
The main question it aims to answer is if individuals with RBD oder PD can follow a combined lifestyle program over six months Participants will take part in a six-month intervention program that includes: Physical training, Mediterranean diet counseling, Sleep counseling and cognitive training.
The program will be supported by psychoeducation, skills training, and personalization to make it practical and motivating.
Eligibility criteria
Qualifiers
All participants: ability to perform informed consent; age 30-85
RBD group: polysomnographic proven diagnosis of isolated REM sleep behavior disorder (iRBD)
PD group: early to moderate disease (Hoehn & Yahr stage 1-2.5), diagnosis according to the Movement Disorder Society diagnostic criteria for clinical Parkinson's Disease
Agreement to participate in group sessions and online meetings
Disqualifiers
dementia (Mini Mental Score, MMSE < 19 points) (MMSE is specifically chosen here to avoid too frequent repetitions of the MoCA, which is used as an outcome parameter for the interventional trial)
physical inability to perform exercise training or other trainings as judged by a physician
manifest (severe) depression (Beck Depression Inventory, BDI-II > 29 points)
participation in other interventional trials
Trial design
Treatments tested in this trial
- Multidomain lifestyle intervention
Treatment groups
Locations
Sponsors and collaborators
University Hospital Schleswig-Holstein
Lead sponsor
University Hospital, Bonn
Collaborator
University of Cologne
Collaborator
Philipps University Marburg
Collaborator
University of Kiel
Collaborator