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Search / Trial NCT05103618

Effect of Meditation and Controls and Subjects With Parkinson's Disease on Brain Activity Measured by fMRI With FDOPA

Launched by ANDREW NEWBERG · Oct 21, 2021

Trial Information

Current as of June 27, 2025

Not yet recruiting

Keywords

Alternative Medicine Complementary Medicine Parkinson's Disease Neurodegenerative Diseases Idiopathic Parkinson's Disease Central Nervous System Diseases Movement Disorders [F 18] Fluorodopa Magnetic Resonance Spectroscopy Pet Positron Emission Tomography Dopaminergic Function

ClinConnect Summary

This clinical trial is looking at how a special type of meditation called orgasmic meditation (OM) affects brain activity in people with Parkinson's disease. Researchers will use advanced imaging techniques, including FDOPA PET scans and MRI, to understand how this meditation might influence dopamine function and markers of inflammation and stress in the brain. The goal is to learn more about the potential benefits of meditation for individuals living with Parkinson's.

To participate, you need to be at least 25 years old and physically able to walk independently. If you have Parkinson's disease, you should be a woman aged 30 or older who is stable on your medication. If you don't have Parkinson's, you can still join as a healthy partner in a couple. Participants will need to confirm they are not pregnant and practice effective contraception during the study. This trial is not yet recruiting, but once it starts, participants can expect to undergo brain scans and take part in meditation sessions, contributing to important research that could help others with Parkinson's in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:(Control Group: 6 healthy, normal couple pairs)
  • 1. No clinical diagnosis of PD
  • 2. Age 25 years old and older
  • 3. Physically independent, ambulatory
  • 4. Women of childbearing potential will confirm a negative pregnancy test and must practice effective contraception during the period of pilot study. In addition, male subjects who have a partner of childbearing age should practice effective contraception.
  • Inclusion Criteria for Female Partner in Couple Pairs in Parkinson's Group who has Parkinson's Disease
  • 1. Clinical diagnosis of PD in female partner
  • 2. Age 30 years old and older
  • 3. Physically independent, ambulatory
  • 4. Hoehn and Yahr score of I-III inclusive.
  • 5. On stable antiparkinsonian medication for at least one month
  • 6. Women of childbearing potential will confirm a negative pregnancy test and must practice effective contraception during the period of pilot study. In addition, male subjects who have a partner of childbearing age should practice effective contraception.
  • Inclusion Criteria for Second Partner with No PD in Couple Pairs in Parkinson's Group
  • 1. No clinical diagnosis of PD
  • 2. Age 25 years old and older
  • 3. Physically independent, ambulatory
  • 4. Women of childbearing potential will confirm a negative pregnancy test and must practice effective contraception during the period of pilot study. In addition, male subjects who have a partner of childbearing age should practice effective contraception.
  • Exclusion Criteria: (In Control Couple Pairs and in Couple Pairs Group in which the Female member has PD)
  • 1. Previous brain surgery.
  • 2. Cognitive impairment by evaluation or known score on Mini-Mental Status examination of 25 or lower.
  • 3. Wheelchair-bound or bed-ridden, non-ambulatory.
  • 4. Intracranial abnormalities that may complicate interpretation of the brain scans (e.g., stroke, tumor, vascular abnormality affecting the target area).
  • 5. Diagnosis of traumatic brain injury with significant impairment.
  • 6. Any medical disorder or physical condition that could reasonably be expected to interfere with the assessment of parkinsonian syndrome symptoms, or with any of the study assessments including the PET-MRI imaging.
  • 7. No metal in their body that would prevent MRI scanning (as determined by the PI).
  • 8. Subjects with evidence of a significant psychiatric disorder by history/examination that would prevent completion of the study will not be allowed to participate.
  • 9. Subjects with current alcohol or drug abuse.
  • 10. Pregnant or lactating women.
  • 11. Enrollment in active clinical trial/ experimental therapy within the prior 30 days.
  • 12. Pending surgery during the course of the study.
  • 13. History of thrombocytopenia or clotting disorders.
  • 14. Cancer patients receiving active chemotherapy.
  • 15. History of uncontrolled diabetes and/or thyroid conditions.
  • 16. History of severe kidney disease (if a subject reports this problem, a serum creatinine will be checked to assess glomerular filtration rate (GFR) and if it is less than 30, they will be excluded).

About Andrew Newberg

Andrew Newberg is a distinguished clinical trial sponsor known for his pioneering research in the fields of neuroscience and psychology, particularly focusing on the intersection of brain function and spirituality. With a robust background in nuclear medicine and a commitment to innovative clinical studies, Newberg seeks to advance understanding of how various cognitive and spiritual practices impact mental health and wellbeing. His work often integrates cutting-edge imaging techniques and empirical methodologies to explore the neurological underpinnings of consciousness, providing valuable insights that contribute to both clinical practice and academic discourse.

Locations

Philadelphia, Pennsylvania, United States

Patients applied

0 patients applied

Trial Officials

Daniel A Monti, MD,MBA

Study Chair

TJU, Integrative Medicine and Nutritional Sciences

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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