Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
FEMALE
NCT06546033

Intermittent Fasting and Mediterranean Diet in Patient With Multiple Sclerosis

Led by Nigde Omer Halisdemir University · Updated on 2024-08-09

34

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

Sponsors

N

Nigde Omer Halisdemir University

Lead Sponsor

A

Acibadem University

Collaborating Sponsor

AI-Summary

What this Trial Is About

When the literature was reviewed, there is no study in which the effects of intermittent fasting and Mediterranean diet on quality of life, sleep, circadian rhythm and appetite hormones leptin and ghrelin levels in MS patients were evaluated and the two diet types were comparatively examined in terms of all these parameters.

CONDITIONS

Official Title

Intermittent Fasting and Mediterranean Diet in Patient With Multiple Sclerosis

Who Can Participate

Age: 18Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female between 18 and 65 years old diagnosed with MS by a physician
  • Not currently in an attack period
  • Not in menopause
  • No autoimmune disease other than MS that affects the study
  • Not following Mediterranean diet or intermittent fasting in the past 3 months
  • No diagnosis of eating behavior disorder
  • No communication problems
  • Signed informed consent form
  • Brain MRI within the last 3 months
  • Not pregnant or lactating
  • No physical disability
  • No history of cancer
  • Body Mass Index between 18.5 and 29.9 kg/m2
  • No loss of 5% or more body weight in the last month
Not Eligible

You will not qualify if you...

  • Diagnosis of autoimmune disease other than MS that affects the study
  • Currently in an attack period
  • Under 18 or over 65 years old
  • In menopause
  • Following Mediterranean diet or intermittent fasting in the last 3 months
  • Receiving diet therapy affecting the autoimmune system in the last 3 months
  • Diagnosed with eating behavior disorder
  • Communication problems
  • Did not sign informed consent
  • Unable to adapt to the study or behaviors adversely affecting participation
  • Used nutritional interventions in the last 3 months
  • Taking supplements like selenium, zinc, iron, vitamin D, or B12 affecting the study
  • History or current cancer treatment
  • Other neurological diseases such as Parkinson's, epilepsy, Alzheimer's
  • Diagnosed with disease lasting more than 4 months in the last 12 months
  • Following specialized dietary patterns (high protein, ketogenic, low energy <1000 kcal/day)
  • Body Mass Index less than 18.5 or greater than 30 kg/m2
  • Lost 5% or more body weight in the last month
  • Having a physical disability

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Nigde Omer Halisdemir University

Niğde, Bor, Turkey (Türkiye), 51200

Actively Recruiting

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Research Team

E

Elif Gökçe İnbaşı, MSc.

CONTACT

N

Nihan Çakır Biçer, PhD.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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