Previous work showed that a shift in functional connectivity from the posterior to the anterior putamen can be seen in PD patients (Helmich et al. 2010). Thus, PD patients probably use their anterior putamen for both cognitive and simple motor tasks…
ID
Bron
Verkorte titel
Aandoening
Parkinson's Disease
Ondersteuning
Performer = Radboud University Nijmegen Medical Centre
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The main study parameter is the change in blood oxygenation level dependent (BOLD) signal in the bilateral anterior putamen during performance of a dual task containing a lower limb motor task and a cognitive task (functional MRI, pre-training vs. post-training assessment).
Achtergrond van het onderzoek
In this trial, which is part of the Seventh Framework program V-TIME, neural correlates of plasticity of the V-TIME fall prevention intervention are investigated.
Doel van het onderzoek
Previous work showed that a shift in functional connectivity from the posterior to the anterior putamen can be seen in PD patients (Helmich et al. 2010). Thus, PD patients probably use their anterior putamen for both cognitive and simple motor tasks. In healthy persons, cognitive tasks mostly rely on the anterior putamen whereas simple motor tasks mostly rely on the posterior putamen. We hypothesize that a bottleneck in the anterior putamen causes reduced dual task performance in PD patients. Through the VR training, we expect to see compensation for this bottleneck in other brain regions. Thus, we hypothesise that treadmill training with VR will cause a partial shift of cognitive control from the anterior putamen towards other brain regions such as the anterior cingulated cortex, the nucleus caudatus and the prefrontal cortex.
Onderzoeksopzet
Pre assessment (all outcome measures), intermediate assessments after 4 weeks (physical and mental functioning) and 6 weeks (physical and mental functioning and fNIRS) of training, post assessment (all outcome measures), 1 and 6 month follow up assessments (all outcome measures besides (f)MRI and fNIRS).
Onderzoeksproduct en/of interventie
At RUNMC (Nijmegen) 50 patients with PD will be randomized into one of these two groups:
1. Treadmill Training with Virtual Reality (TT+VR) for 12 weeks, three times per week;
2. Active control comparison of Treadmill Training alone (TT), 12 weeks, three times per week.
At TASMC (Tel Aviv) 40 patients with PD will be randomized into one of these two groups:
1. Treadmill Training with Virtual Reality (TT+VR) for 6 weeks, three times per week;
2. Active control comparison of Treadmill Training alone (TT), 6 weeks, three times per week.
Publiek
Department of Geriatric Medicine, 925<br>
PO box 9101
Freek Nieuwhof
Nijmegen 6500 HB
The Netherlands
+31 (0)24 3617853
F.Nieuwhof@ger.umcn.nl
Wetenschappelijk
Department of Geriatric Medicine, 925<br>
PO box 9101
Freek Nieuwhof
Nijmegen 6500 HB
The Netherlands
+31 (0)24 3617853
F.Nieuwhof@ger.umcn.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. At least 2 falls within the 6 months prior to the study;
2. Age range: 60-85 years;
3. Diagnosis of PD (UK Parkinson's Disease Society Brain Bank: UKBB);
4. Hoehn and Yahr stage II-III (on medication);
5. Stable medication for at least one month and anticipated for the next 6 months;
6. Able to walk at least 5 minutes unassisted;
7. Adequate hearing and vision.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Psychiatric co-morbidities (e.g., major depression - Diagnostic and Statistical Manual of Mental Disorders (DSM) IV criteria);
2. Clinical diagnosis of dementia (e.g., Alzheimer's, vascular, etc.);
3. History of stroke, traumatic brain injury, brain tumour or other neurological disorders;
4. Acute lower back or lower extremity pain, musculoskeletal injuries, peripheral neuropathy which restricts gait;
5. Unstable medical condition including cardiovascular instability in past 6 months;
6. Unable to comply with training;
7. Cognitively impaired (< 24 on Mini-Mental State Examination);
8. Interfering therapy, or fall clinic visit <1 months ago;
9. Severe freezing precluding safe participation (>15 on New Freezing of Gait Questionnaire);
10. Metal objects or fragments in/on body;
11. Active implant (e.g. pacemaker, neurostimulator, insulin pump);
12. Epilepsy;
13. Claustrophobia.
Opzet
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Register | ID |
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NTR-new | NL3488 |
NTR-old | NTR3723 |
CCMO | NL41661.091.12 |
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OMON | NL-OMON36978 |