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Recruiting NCT07790744

NCT07790744 A Comprehensive, Multimodal Characterization of Prodromal PD in Subjects With RBD

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Clinical Trial Summary
NCT ID NCT07790744
Status Recruiting
Phase
Sponsor Danish Research Centre for Magnetic Resonance
Condition REM Sleep Behavior Disorder
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2026-02-01
Primary Completion 2028-06-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2026-02-01 with a primary completion date of 2028-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Comprehensive characterization of early-stage Parkinson's disease in patients with REM sleep behavior disorder Parkinson's disease (PD) is the fastest-growing neurodegenerative disorder worldwide, significantly affecting quality of life and causing substantial social and economic burdens. Currently, treatments for Parkinson's disease primarily manage symptoms through medication and lifestyle changes but cannot stop disease progression. By the time Parkinson's disease is diagnosed, substantial nerve-cell loss has already occurred in specific brain areas. Identifying early signs of PD before symptoms fully develop is essential for improving future treatment strategies. This research project aims to deeply understand the earliest stages of Parkinson's disease by studying patients with REM sleep behavior disorder (RBD). RBD is a condition characterized by unusual movements or behaviors during dream sleep, caused by nerve-cell loss in the brainstem. Importantly, more than 80% of individuals with RBD eventually develop Parkinson's disease or related conditions, such as Dementia with Lewy Bodies or Multiple System Atrophy. Study Goals: Our study will examine multiple potential biomarkers (measurable indicators) that could help identify early stages of Parkinson's disease. These include: 1. Brain structure changes: The Investigators will use advanced imaging methods (7-Tesla MRI) to closely examine specific brain regions known to be affected early in Parkinson's disease, particularly the substantia nigra and the locus coeruleus (LC). The LC helps regulate sleep and wakefulness, and studies have shown it is damaged in patients with RBD and Parkinson's disease. Additionally, the investigators will use specialized imaging (Pe2i-PET and MIBG-scintigraphy) to measure dopamine availability and changes in heart nerve function. 2. Abnormal protein buildup (ɑ-synuclein): In Parkinson's disease, nerve-cell death is linked to abnormal clumping of a protein called ɑ-synuclein within cells. Detecting this abnormal protein buildup early might help identify who is at risk of developing Parkinson's disease. The investigators aim to explore how levels of ɑ-synuclein aggregation relate to other early signs of the disease. 3. Functional changes in brain and body: Polysomnography, an overnight sleep test recording brain (EEG) and heart (ECG) activity, is the best method for diagnosing RBD. The investigators will also measure brain activity during wakefulness to further understand early changes. 4. Symptoms and physical tests: Participants will undergo thorough clinical assessments, including motor and cognitive tests, as well as tests evaluating autonomic (automatic nervous system) function, such as cardiovascular responses using a tilt-table test. Together, these extensive assessments will provide a detailed understanding of how Parkinson's disease begins and progresses. This knowledge can greatly improve early diagnosis, allowing earlier and potentially more effective treatments for individuals at high risk. Study Design: The investigators will recruit: * 50 individuals diagnosed with REM sleep behavior disorder * 50 control participants without major psychiatric or neurological disease, matched by age and gender THe investigation team have a complete, detailed plan and will begin collecting data as soon as ethical approval is granted. Main Hypotheses: Although our extensive data will allow many analyses, the investigation team specifically predict: * Individuals with RBD will show more significant damage in the locus coeruleus compared to controls. * Greater damage in the locus coeruleus will correlate with more severe cognitive issues, sleep problems, and autonomic dysfunction. * Cognitive issues in RBD patients might correlate with specific patterns of damage in different parts of the locus coeruleus. For example, memory problems might be linked to more damage in the front (rostral) part of this region. Impact: This study will significantly enhance early detection of Parkinson's disease, paving the way for personalized medical approaches and potentially more effective treatments. Conducted by a multidisciplinary team of experts in brain imaging, sleep medicine, autonomic function, and protein aggregation, this research supports Denmark's leadership in precision clinical imaging and aligns closely with hospital research strategies aimed at understanding and treating chronic diseases. Ultimately, our goal is to improve personalized patient care for Parkinson's disease in the future.

Eligibility Criteria

Inclusion Criteria: Both groups - The ability to give informed consent For RBD-group * Verified REM-sleep behaviour disorder via polysonography * No other significant neurological and psychiatric ilness For Healthy controls \- Age matched to RBD-group Exclusion Criteria: * Ferrous objects in or around the body * Pacemaker or other implanted electronic devices * Drug abuse unrelated to medication or alcohol abuse over a period of 6 months prior to the experiment * Other major immunological, cardiac, neurological or neuropsychiatric disorders * Claustrophobia * Incapability of giving informed consent * Unwillingness to be informed about abnormal findings. * Participation in clinical trials involving drug testing over a period of 6 months prior to the experiment. * Disease symptoms leading to excessive movement inside the scanner (e.g., excessive tremor)

Contact & Investigator

Central Contact

Sune G Thomsen, MD

✉ sune.gram.thomsen.01@regionh.dk

📞 +4552176251

Frequently Asked Questions

Who can join the NCT07790744 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying REM Sleep Behavior Disorder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07790744 currently recruiting?

Yes, NCT07790744 is actively recruiting participants. Contact the research team at sune.gram.thomsen.01@regionh.dk for enrollment information.

Where is the NCT07790744 trial being conducted?

This trial is being conducted at Hvidovre, Denmark.

Who is sponsoring the NCT07790744 clinical trial?

NCT07790744 is sponsored by Danish Research Centre for Magnetic Resonance. The trial plans to enroll 100 participants.

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