NCT06705517Recruiting
Mediterranean Diet Effects on Parkinson's Disease
Mediterranean Diet Effects on Parkinson's Disease (MED-PARK): a Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 11 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Currently, there are no disease-modifying treatments for Parkinson's disease (PD), the second most common neurodegenerative disorder worldwide, making it crucial to find interventions that can change the disease's trajectory. Epidemiological studies suggest that the Mediterranean diet (MD) is linked to improved motor and non-motor symptoms, slower disease progression, and lower mortality in PD patients. However, few interventional studies have explored this connection. This study assesses whether an MD can improve motor and non-motor symptoms in PD patients. Additionally, the study will examine the effects of the diet on a patient's quality of life, gastrointestinal symptomatology, adaptive immune system, fecal and nasal microbiome, and fecal and urinary metabolomics. This is a randomized, controlled, non-pharmacological, single-center, masked trial with two parallel groups. It will evaluate the safety and efficacy of the MD on motor and non-motor symptoms reported by PD patients. Forty-four participants, aged 40-85, meeting the inclusion criteria will be enrolled and block-randomized into two groups: one maintaining their usual diet (control) and the other following a MD for six months (intervention). The primary outcome is patient-reported symptoms, measured using the MDS-UPDRS I+II score. Secondary outcomes include the analysis of adaptive immune system cells, nasal and fecal microbiome composition, and inflammatory and metabolic markers. Additional assessments include disease severity (MDS-UPDRS), non-motor symptoms (Non-Motor Symptoms Scale), participant well-being (36-Item Short Form Health Survey), gastrointestinal symptoms (Gastrointestinal Symptom Rating Scale and Patient Assessment of Constipation Quality of Life), and the intensity of dopaminergic therapy (levodopa equivalents). Evaluations will be performed at baseline and after six months.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 44 (estimated)
- First submitted
- 14 Nov 2024
- Start date
- 17 Jan 2025
- Primary completion date
- Feb 2026
- Lead sponsor
- Università degli Studi dell'Insubria
- Diseases
- Parkinson disease
- NCT number
- NCT06705517
What you commit to
- Study type: Interventional
- Planned participants: 44
- From 17 Jan 2025 to the primary completion date, Feb 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Chronic use of immunosuppressive drugs in the past year;
- Concurrent participation in other interventional studies;
Other illness
- Chronic autoimmune diseases;
- Chronic use of cytotoxic cancer drugs in the past year;
Other
- Atypical or secondary parkinsonism;
- Underweight (\<18.5);
- Obesity (BMI\>30);
- Pregnancy or suspected pregnancy;
- Normal assisted nutrition;
- Enteral nutrition;
- Major abdominal surgeries;
- Intentional change in diet after PD diagnosis.
Who the study is looking for
- PD diagnosis according to international guidelines;
- Age between 40 and 85 years;
- Naive to medication or with a stable dosage of anti-Parkinson's therapy for at least two weeks;
- Hoehn \& Yahr stage ≤3;
- Normal independent feeding;
- Ability to complete informed consent;
- Willingness to maintain the usual diet in the period between T0 and T1;
- Willingness to maintain the usual diet if randomized to the control group in the T1-T2 period;
- Willingness to make changes in their diet to follow a Mediterranean diet if randomized to the intervention group in the T1-T2 period;
- Willingness to fill out questionnaires;
- Willingness to provide blood samples during the study collection periods;
- Willingness to provide stool samples during the study collection periods;
- Willingness to fast (without food or drink except water, tea or coffee) at least 12 hours before each sample collection;
- Willingness to discontinue taking supplements, probiotics, herbal or high- dose vitamins or minerals that could impact inflammation during the period between T0 and T1 and for the duration of the study protocol;
- No medical and/or social conditions that could interfere with participation in a six-month interventional study.
Age in the registry: 40 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Centre for Research in Medical Pharmacology Coordinator of this site? Confirm its status | Varese | Italy | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.