Neural Correlates of Impulsivity in Idiopathic REM Sleep Behavior Disorder

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Recruiting
CT.gov ID
NCT05353855
Collaborator
(none)
96
1
36
2.7

Study Details

Study Description

Brief Summary

This study aims to investigate the neural correlates (structural changes, functional connectivity, and structural connectivity of brain structures in prefrontal cortex and basal ganglia) of impulsivity by measuring structures and the blood-oxygen-level-dependent signal of brain in response to impulsive tasks and task-free using functional Magnetic Resonance Image method among healthy controls, patient with prodromal PD (iRBD), and patients with PD.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Detailed Description

Background: Excessive impulsivity is an important non-motor symptom of Parkinson's disease (PD), especially for those on dopamine agonist treatment. Dopaminergic dysfunction has been highly correlated with impulsivity. Given that idiopathic REM sleep behavior disorder (iRBD) is a prodromal stage of alpha-synucleinopathy, such as PD, the dysfunction of dopaminergic system at this early stage may also precipitate alternation of impulsivity.

Hypothesis and objectives: iRBD may have altered impulsivity which is similar to that found in de novo PD and may serve as a biomarker in differentiating iRBD from healthy controls. This study aims to investigate the neural correlates (structural changes, functional connectivity, and structural connectivity of brain structures in prefrontal cortex and basal ganglia) of impulsivity by measuring structures and the blood-oxygen-level-dependent signal of brain in response to impulsive tasks and task-free using functional Magnetic Resonance Image method among healthy controls, patient with prodromal PD (iRBD), and patients with PD.

Design and subjects: This is a case-control study that will recruit 96 subjects (24 healthy controls, 24 patients with iRBD, 24 PD patients on dopaminergic medication and 24 PD patients who are not on dopaminergic medication).

Main outcome measures: 1) The difference in brain activity in response to impulsivity tasks between groups; 2) The difference in structure volume, structural and functional connectivity of region of interest related to impulsivity (prefrontal cortex and basal ganglia) between groups; 3) The association of these changes with the stage of disease from healthy, to prodromal, and to clinically diagnosed PD.

Study Design

Study Type:
Observational
Anticipated Enrollment :
96 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Neural Correlates of Impulsivity in Idiopathic REM Sleep Behavior Disorder: a Functional Magnetic Resonance Imaging Case-control Study
Actual Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Early unmedicated PD patients converted from iRBD

Chinese aged 50 or above; Being capable of giving informed consent for participation of the study; Having a diagnosis of PD confirmed by neurologists according to the United Kingdom Parkinson's Disease Survey Brain Bank. Onset of PD motor symptoms of < 3 years; In view of the heterogeneity of PD, the investigator will only include those patients with RBD preceding the onset of motor symptoms of PD. Drug naïve (dopaminergic medications have not been started)

Other: No intervention
No intervention

Early medicated PD patients converted from iRBD

Inclusion criteria will be the same as that of early unmedicated PD except that they should be on dopaminergic medications.

Other: No intervention
No intervention

iRBD patients

Chinese aged 50 or above; Being capable of giving informed consent for participation of the study; Having a diagnosis of RBD according to the International classification of sleep disorder 3rd edition (ICSD 3rd), fulfilling both the clinical and video-polysomnography (vPSG) criteria.

Other: No intervention
No intervention

Healthy controls

Age-and sex-matched with the groups; Being capable of giving informed consent for participation of the study; Without a personal history or a family history of PD or RBD; A total score on REM Sleep Behavior Questionnaire (RBDQ-HK) less than 19, which is the suggestive cut-off of a diagnosis of RBD; Absence of self-report dream enactment behaviors and RSWA as measured by v-PSG.

Other: No intervention
No intervention

Outcome Measures

Primary Outcome Measures

  1. Brain activity [1 year]

    To access different cognitive aspects in neurobehavioral impulsivity such as BART, TCIP and SKIP between groups

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Age-and sex-matched with the groups;

  2. Being capable of giving informed consent for participation of the study;

  3. Without a personal history or a family history of PD or RBD;

  4. A total score on REM Sleep Behavior Questionnaire (RBDQ-HK) less than 19, which is the suggestive cut-off of a diagnosis of RBD;

  5. Absence of self-report dream enactment behaviors and RSWA as measured by v-PSG

Exclusion Criteria:
  1. Having a history of ICD diagnosis or ICD symptom(s) assessed with Questionnaire for Impulsive-Compulsive Disorders in Parkinson's Disease-Rating Scale (QUIP-RS);

  2. Presence of narcolepsy or other neurodegenerative diseases (except for PD group) that may give rise to RBD;

  3. Presence of mood disorder which may have great impact on impulsivity;

  4. A total score of the Montreal Cognitive Assessment (MOCA) ≤ 22 and the Clinical Dementia Rating (CDR) ≥ 1, indicating dementia;

  5. Except for early medicated PD patients, if subjects from other groups who are on medication that may induce impulsivity, such as dopaminergic medication, will be excluded;

  6. Contraindication to MRI (e.g., presence of implants or claustrophobia).

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Chinese University of Hong Kong Hong Kong Hong Kong

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Professor Wing Yun Kwok, Professor, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05353855
Other Study ID Numbers:
  • HMRF08191416
First Posted:
Apr 29, 2022
Last Update Posted:
Aug 24, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Professor Wing Yun Kwok, Professor, Chinese University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2022