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Completed

NCT Number: NCT05119075

Psychological Effects of Levodopa in Parkinson's Disease

The investigators aim is to study neuropsychiatric symptoms and underlying abnormalities in resting-state fMRI in patients with Parkinson's disease (PD) suffering from neuropsychiatric fluctuations, to enhance the understanding of the pathophysiological mechanisms underlying neuropsychiatric symptoms.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Inselspital, Berne, Bern, Switzerland

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About this study

Parkinson's disease (PD) is primarily classified and known as a movement disorder characterized by tremor, bradykinesia and rigidity. However, clinical examination and research have shown that PD extensively affects other systems as well, giving rise to non-motor symptoms (NMS) such as anxiety, sleep disorders, apathy, depression, cognitive impairment, and hallucinations. These non-motor fluctuations (NMF) represent a main source of disability in PD and among those, neuropsychiatric fluctuations are the most frequent. During the dopaminergic OFF-drug state anxiety, apathy, and depression are common, whereas during the dopaminergic ON-drug state euphoria, well-being, impulse control disorders (ICD) and other behavioral addictions, mania, and psychosis might occur.

Despite the severe consequences associated with dopaminergic modulation, the understanding of the pathophysiological mechanisms of neuropsychiatric symptoms is still limited and better detection and more effective treatments are needed. Fluctuating PD is a very powerful model allowing to study opposite psychiatric states intra-individually in both levodopa dopaminergic ON- and OFF-drug state, allowing to abstract many interpersonal variables.

Neurotechnology and advanced neuroimaging techniques can improve the understanding of the neural basis and brain mechanisms of specific neuropsychiatric symptoms in PD. In particular, dynamic functional connectivity (FC) analysis characterizes functional abnormalities from resting state (rs)-fMRI not only in terms of brain activations, but also of whole-brain functional networks and the transitions between maps of activations. The temporal evolution of these networks, assessed with dynamic FC approaches, has recently shown to be relevant in several clinical contexts.

Therefore, the investigators long-term goal is to identify specific resting-state signatures/biomarkers for the individual neuropsychiatric PD symptoms related to disease in dopaminergic OFF-drug state (depression, anxiety, apathy, fatigue, shame, bradyphrenia) and to dopaminergic treatment in dopaminergic ON-drug state (mania, impulse control disorders, hallucinations, psychosis, creative thinking), which might be used in the future as a proxy for the measurement of neuropsychiatric symptoms/fluctuations and thus to assess the effectiveness of specific therapies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults above 18 years old
  • Male or female
  • Diagnosed with Parkinson's disease
  • Able to understand instructions, neuropsychological tests and provide written informed consent
  • Able to understand the locally used language of the experimental site and speak fluently
  • Presence of neuropsychiatric fluctuations, defined as the sum ≥ 3 of items included in the Ardouin Scale of Behaviour in Parkinson's Disease (ASBPD) part 2

Exclusion criteria

  • Structural brain disease other than Parkinson's disease
  • Substance abuse and/or dependence (other than DRT)
  • Ongoing depression with suicidal ideation
  • Severe tremors/dyskinesia/ interfering with MRI performance
  • Participating in a pharmacological study
  • Inability to provide informed consent (legal guardianship)
  • MRI contraindications
  • Pregnancy

Treatment and study plan

Dopaminergic OFF-drug state

Other

Dopaminergic OFF-drug state: Overnight withdrawal of dopaminergic antiparkinsonian drugs during visit 3 or 4. The sequence of drug conditions (dopaminergic OFF-drug/ON-drug state or ON-drug/OFF-drug state) will be randomized.

Dopaminergic ON-drug state

Other

Dopaminergic ON-drug state: Patient will be evaluated in his/her regular treatment in dopaminergic ON-drug state at visit 3 or 4. The sequence of drug conditions (dopaminergic OFF-drug/ON-drug state or ON-drug/OFF-drug state) will be randomized.

Primary outcomes

  1. Correlation of functional connectivity abnormalities with neuropsychiatric fluctuations

    Time frame: ≤ 6 weeks

    Score on the Neuropsychiatric Fluctuations Scale (NFS)

  2. Correlation of functional connectivity abnormalities with shame

    Time frame: ≤ 6 weeks

    Score on the Shame Visual Analogic Scale

  3. Correlation of functional connectivity abnormalities with hallucinations

    Time frame: ≤ 6 weeks

    Score on robot-induced presence hallucination (PH) ratings

  4. Correlation of functional connectivity abnormalities with bradyphrenia

    Time frame: ≤ 6 weeks

    Score on the Bradyphrenia Scale

  5. Correlation of functional connectivity abnormalities with creativity

    Time frame: ≤ 6 weeks

    Score on the Creative Thinking Scale

Secondary outcomes

  1. The role of dopamine on hallucinations

    Time frame: ≤ 6 weeks

    Measurement of the influence of dopamine on hallucinations using the robot-induced presence hallucination (PH) ratings. Assessments will be performed under the two conditions (dopaminergic ON and OFF drug state) and compared. The higher the score, the more hallucinations are experienced by patients.

  2. The role of dopamine on creativity

    Time frame: ≤ 6 weeks

    Measurement of the influence of dopamine on the Creative Thinking Scale. Assessments will be performed under the two conditions (dopaminergic ON and OFF drug state) and compared. The higher the score, the more creative the patients are.

  3. The role of dopamine on shame

    Time frame: ≤ 6 weeks

    Measurement of the influence of dopamine on the Shame Visual Analogic Scale. Assessments will be performed under the two conditions (dopaminergic ON and OFF drug state) and compared. The higher the score, the more shame patients feel.

  4. The role of dopamine on bradyphrenia

    Time frame: ≤ 6 weeks

    Measurement of the influence of dopamine on the bradyphrenia scale. Assessments will be performed under the two conditions (dopaminergic ON and OFF drug state) and compared. The higher the score, the more bradyphrenic the patients are.

Sponsors and collaborators

Lead sponsor

Insel Gruppe AG, University Hospital Bern

Other

Collaborators

  • Ecole Polytechnique Fédérale de Lausanne
  • University Hospital, Geneva

Registry information

Official study title

Unravelling the Impact of Levodopa on Dysfunctional Brain Networks in Parkinson's Disease With Neuropsychiatric Fluctuations

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Nov 12, 2021
Registry last updated
Apr 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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