High Frequency and Intensive Prevention Program

Not Applicable

Completed

• Conditions: Parkinson Disease

• Registration Number: NCT04103255
• Lead Sponsor: University Hospital, Basel, Switzerland

Brief Summary

The treatment of PD has made considerable advances in recent years with respect to drug therapies, as well as many new physiotherapy and drug-based methods, and there have also been great improvements in therapy thanks to deep brain stimulation. Cognitive rehabilitation has shown to be effective in PD (Abbruzzese et al., 2016), however, there has yet to be a major breakthrough in the treatment and prevention of PDD (Parkinson's Disease Dementia ). This is where the high frequency and intensive prevention described here comes into play.

Detailed Description

Cognitive decline is an important and common complication in Parkinson's Disease (PD); approximately 27% of non-demented PD patients have Mild Cognitive Impairment (MCI) (Litvan et al. 2012, Chaudhuri et al., 2011) and up to 80% develop PD dementia (PD-D) over the long term (Hely et al., 2005). Cognitive course in PD is heterogeneous and affects visuospatial, attentional, executive and memory function; studies report different cognitive subtypes and divergent patterns of cognitive decline (Kehagia et al., 2010; Litvan et al., 2011; Williams-Gray et al., 2007; Yarnall et al., 2014). Recently, models have been constructed to estimate individual risk for global cognitive impairment using a small set of predictor variables (Liu et al. 2017; Velseboer et al., 2016). These prediction algorithms were developed in large samples of PD patients and accurately forecast cognitive decline in both, patients with MCI and patients with PD-D and were successfully replicated in independent samples; a score with a predefined cut off point predicts dementia with high positive and negative predictive values (Liu et al., 2017).

The primary aim of this study is the possible stabilization or delay of cognitive decline as well as the improvement of the quality of life of the patients. As secondary outcome, the change in symptoms associated with PD, will be investigated. Psychological states as depression and anxiety, as well as cognitive performance in different areas, for example attention and memory shall be investigated. Neurological symptoms, for example motor function and sleepiness, will also be assessed as secondary parameters and potentially confounding factors.

This study is a 4 week non-randomized controlled trial with one intervention group (HIPP) and one control group (CogniPlus). Primary and secondary outcome measures are assessed at baseline and are repeated after the 4-week intervention period and at 6 month in a follow-up assessment. After 4 weeks there is an intermediate measurement consisting of the primary outcome measures.

The intervention group receives individualized program: the program will be tailored to the patient's needs, strengths and weaknesses, resulting from the initial assessment.

1. Tai Chi - "Keep Moving" is an exercise programme for patients with movement disorders that explicitly utilizes the health aspect of Tai Chi movement teachings. Each session lasted 60 minutes and ended with a 10-minute meditation. The Tai Chi sessions in our study were carried out twice a week under the guidance of certified Tai Chi instructors. Details of this program can be found on the following website: https://taiji-therapie.ch/

2. CogniFit® - is a online-based personalized cognition training program. This well-validated cognitive training improves attention, working memory, memory, executive function, and visual perceptual functions. Each session lasted 20 minutes and was applied 2-5 times per week based on the results of the baseline tests. The home-based approach took place under the supervision of a psychologist or a specially trained psychology student. The difficulty level was automatically adjusted by the program itself. Details of the program can be found on the following website: https://www.cognifit.com/.

3. SpeechCare - (MoveApp) is a home-based approach for patients with Parkinson's disease. The training program uses automatic speech recognition (ASR) and thus can provide feedback on speech intelligibility. Each session lasted 12 minutes and was conducted 1-3 times per week based on the results of the baseline test of SpeechCare . The domestic approach took place under the supervision of a psychologist or a specially trained psychology student. The level of difficulty was manually adjusted as needed. Details of the program can be found on the following website: https://www.speechcare.de/.

The patients in the control group received a computer-assisted cognitive training program: CogniPlus (Schuhfried GmbH, Vienna, Austria). Each training session consisted of different tasks (Focused attention; working memory; planning and action skill; respons inhibition) that were performed for 10 Minutes each. Details of the program can be found on the following website: www.schuhfried.at. The training sessions were supervised by a psychologist or a specially trained student of psychology

Study Timeline

• Study First Submitted: 2019-09-17
• Study First Submitted QC: 2019-09-24
• Study First Posted: 2019-09-25
• Study Start: 2020-07-10
• Primary Completion: 2021-11-01
• Study Completion: 2022-02-01
• Status Verified: 2023-01
• Last Update Submitted: 2023-01-04
• Last Update Posted: 2023-01-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 28

Inclusion Criteria

• Patients with idiopathic Parkinson syndrome according to United Kingdom Parkinson's Disease Brain Bank Criteria
• mental competence to provide informed consent
• able to understand German sufficiently

Exclusion Criteria

• Severe dementia (DMS-IV, mini mental Status (MMS) <24, moca test (MoCa) <21)
• young onset Parkinson's disease (<18y)
• other neurological or psychiatric diseases of the brain not related to PD
• secondary parkinsonism
• physical impairment hindering the adequate execution of the training
• insufficient knowledge of German
• pregnancy
• Deep Brain Stimulation (DBS) is no exclusion criterion.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Attention: Trail Making Test, part A (J. Perianez et al., 2007)	Before and after 4 weeks of training, After 6-month	Trail Making Test, part A serve to evaluate the attention
Episodic memory: California Verbal Learning Test (CVLT; Delis, Kramer, Ober, & Kaplan, 1987)	Before and after 4 weeks of training, After 6-month	This is a method that tests memory functions, including encoding, retrieval, and recognition processes. The task is to learn in five cycles a shopping list of 16 words assigned to four semantic categories (i.e. beverages, fruits, clothing, tools). As many words as possible should be enumerated after each cycle. The sum of the words stored in the 1-5 cycles is used as the encoding parameter.
working memory: Corsi Block Test (Härtig et al., 2000)	Before and after 4 weeks of training, After 6-month	Corsi Block Test serve to evaluate the verbal and visual working memory. In the Corsi Block, the test person is presented with a board with irregularly arranged cubes. The task is to remember a sequence of tapped cubes and then to tap the cubes in the same sequence or later to follow the path shown in reverse order. Also with this test the difficulty increases, as the offered sequences become increasingly longer.; The total score for the Digit Span is the sum of 12 items, ranging from 0 (worst possible result) to 12 (best possible result).; The total score for the Corsi Block is the sum of 14 points in forward typing, ranging from 0 (worst score) to 14 (best symptoms) and the sum of 12 points in backward typing from 0 (worst score) to 12 (best symptoms).
Visuo-construction: Rey-Osterrieth complex figure (Duley et al., 1993)	Before and after 4 weeks of training, After 6-month	The Rey-Osterrieth (ROCF) and Taylor (TCF) complex figure tests are widely used to assess visuospatial and constructional abilities as well as visual/non-verbal Memory (Marie-Pier Tremblay et al., 2015). The score ranging from 0 (worst possible result) to 36 (best possible result).; ·
Executive function (flexibility): Wisconsin Card Sorting test, number of errors (H.E. Nelson, 1976)	Before and after 4 weeks of training, After 6-month	Wisconsin Card Sorting test serve to evaluate the executive function

Secondary Outcome Measures

Name	Time	Method
Electroencephalogram (EEG)	Before and after 4 weeks of training, After 6-month	1. EEG power in Delta; Theta; Alpha 1; Alpha 2; Beta.; 2. Brain Network Connectivity
Unified Parkinson's Disease Rating Scale UPDRS Part III	Before and after 4 weeks of training, After 6-month	This is the standard scale used for grading severity of PD. (UPDRS) - Four Parts Higher score values represent a worse outcome.; Part I: Mentation, Behavior and Mood - 4 questions 1-4 Score range: 1-16; Part II: Activities of Daily Living - 13 questions 5-17 Score range: 0-52 Part III: Motor Examination - 19 questions 18-31 and 25 total assessments Score range: 0-100 Part IV: Complications of Therapy (In the past week) - 11 questions Score range: 0-25
Epworth Sleepiness Scale (M.W. Johns, 1991)	Before and after 4 weeks of training, After 6-month	Measuring Daytime Sleepiness
Near-infrared spectroscopy	Before and after 4 weeks of training, After 6-month	Detecting changes in blood hemoglobin concentrations associated with neural activity
Tinetti Mobility Test (D.A. Kegelmeyer et al., 2007)	Before and after 4 weeks of training, After 6-month	Balance and stability assessment

Trial Locations

Locations (1)

University Hospital Basel; 🇨🇭 Basel, Switzerland