Overview
The aim of the study is to compare the effects of 2 different dosages and modalities of motor-cognitive rehabilitation in Parkinson's disease with postural instability and gait disorders (PD-PIGD) on clinical features, neuroimaging and blood-based biomarkers at short-term (2 months) and long-term (7 months) follow-up. Fifty subjects with PD-PIGD will be randomized in 2 training groups: DUAL-TASK+AOT-MI and the DUAL-TASK groups. The DUAL-TASK+AOT-MI group will perform a dual-task gait/balance training consisting of action observation training (AOT) and motor imagery (MI) combined with practicing the observed-imagined exercises; DUAL-TASK group will perform the same exercises combined with watching landscape videos. The training will last 6 weeks, 3 times/week, 1 hour per session.
Before and after training (W6), all the patients will undergo neurological, gait/balance, cognitive/behavioral, magnetic resonance imaging (MRI) and serum biomarkers evaluations. Neurological, gait/balance, cognitive/behavioral assessments and serum biomarkers will be also repeated at the 14-week follow-up (W14) to assess maintenance of results.
Patients of both DUAL-TASK+AOT-MI and DUAL-TASK groups will be further randomized to repeat the training (6 weeks, 3 times/week, 1 hour each session) starting at W14 (DUAL-TASK+AOT-MI_DOUBLE and DUAL-TASK_DOUBLE groups). After six weeks (W20) all the subjects repeating the training will be evaluated (neurological, gait/balance, cognitive/behavioral assessments). At 28-week follow-up (W28), the whole sample of patients will be assessed with neurological, gait/balance, cognitive/behavioral, MRI and serum biomarkers evaluations. All MRI scans will be acquired at least 12 hours after last dopaminergic therapy administration to mitigate the pharmacological effects on neural activity. Twenty age- and sex-matched healthy controls will be recruited to perform gait/balance and cognitive/behavioral assessments, blood sample and brain MRI acquisition at baseline. The secondary aims of the study are to define the neuroimaging and blood-based biomarkers of PD-PIGD patients presenting different clinical features (e.g. presence of mild cognitive impairment, freezing of gait, falls and mood disturbances) and to evaluate the role of blood-based and neuroimaging biomarkers, together with clinical characteristics, in predicting the response to different dosages of rehabilitation in PD-PIGD throughout the development of a machine-learning algorithm.
Eligibility
Inclusion criteria for PD patients:
- 45 years ≤ age ≤ 85 years;
- Idiopathic PD according to the Movement Disorders Society (MDS) diagnostic criteria
- Hoehn & Yahr (H&Y) score <= 4
- PIGD phenotype
- Stable dopaminergic medication for at least 4 weeks and without any changes during the observation period (28 weeks)
- No dementia according to Litvan's criteria and Mini-Mental Status Examination score (MMSE) >= 24
- No significant tremor/involuntary movements that could determine artifacts during the MRI acquisition
- Oral and written informed consent to study participation
Inclusion criteria for healthy controls:
- sex-matched and age-matched (age range: mean age of PD years ± 15 years);
- oral and written informed consent to study participation
Exclusion criteria:
- Medical conditions or substance abuse that could interfere with cognition;
- Any major systemic, psychiatric, neurological, visual, and musculoskeletal disturbances or other causes of walking inability;
- Contraindications to undergoing MRI examination;
- Brain damage at routine MRI, including lacunae and extensive cerebrovascular disorders;
- Denied oral and written informed consent to study participation.