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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04036552
Other study ID # SMEC_2018-19_028
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 1, 2019
Est. completion date October 3, 2019

Study information

Verified date July 2019
Source St Mary's University College
Contact Leta Pilic, PhD
Phone 0208 240 4000
Email leta.pilic@stmarys.ac.uk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The associations between dietary choline, genetics and anxiety/depression


Description:

Choline, previously considered to be a vitamin, is an essential nutrient involved in a plethora of biological pathways. Choline status is thought to be associated with depression and anxiety, however, the lack of evidence regarding the exact mechanism of its action warrants further investigation. This study aims to explore the associations between dietary choline and depression and anxiety in healthy individuals and how these may differ according to genetics, specifically Phosphatidylethanolamine N-Methyltransferase gene involved in endogenous and exogenous choline metabolism. Establishing these associations could reinforce the need for future intervention trials that could in turn establish causality and determine the mechanistic effects of dietary choline and the PEMT gene activity on depression/anxiety


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 80
Est. completion date October 3, 2019
Est. primary completion date October 3, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Overall healthy males

- pre-menopausal females of 18-50 years of age.

Exclusion Criteria:

- Individuals with a current clinical diagnosis of anxiety and depression

- pregnant or lactating

- post-menopausal women

- individuals suffering with chronic disease (cardiovascular disease, type-2 diabetes mellitus and cancer)

- individuals using choline, lecithin or soy supplements,

- obese individuals with a Body Mass Index (BMI) >30 kg/m2.

Study Design


Locations

Country Name City State
United Kingdom St Mary's University London

Sponsors (1)

Lead Sponsor Collaborator
St Mary's University College

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Depression Hospital Anxiety and Depression questionnaire score higher than 11 1 day observation
Primary Anxiety Hospital Anxiety and Depression questionnaire score higher than 11 1 day observation
Secondary Choline intake Dietary choline intake 3 day observation
Secondary Plasma choline levels Choline levels in plasma obtained by colorimetry 1 measurement
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