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NCT05327322 · ClinicalTrials.gov registry record · NA

Functional Outcomes From Diets in Multiple Sclerosis

A NA study of Relapsing Remitting Multiple Sclerosis and Secondary Progressive Multiple Sclerosis, sponsored by University of Alabama at Birmingham.

Recruiting
Registry status
NA
Development phase
100
Enrollment target
2
Study locations

NCT05327322 is a NA study of Relapsing Remitting Multiple Sclerosis and Secondary Progressive Multiple Sclerosis that is actively recruiting participants, run by University of Alabama at Birmingham. The registered enrollment target is 100 participants, below the 199-participant average among 25 other Relapsing Remitting Multiple Sclerosis trials with a reported enrollment target (50% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT05327322, a NA study of Relapsing Remitting Multiple Sclerosis and Secondary Progressive Multiple Sclerosis, is actively recruiting participants, sponsored by University of Alabama at Birmingham.

RECRUITING
Registry status
NA
Development phase
100 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to test the effects of two dietary interventions, glycemic load and calorie restriction, on physical function, cognition, pain, fatigue, mood, and anxiety in adults with multiple sclerosis (MS). The investigators will also explore the how the diet interventions impact inflammation, immunity, and metabolic biomarkers.

Interventions

  • BEHAVIORAL Glycemic load
  • BEHAVIORAL Calorie restriction
  • BEHAVIORAL Behavioral support

Study Locations (2)

Alabama

  • University of Alabama at Birmingham - Birmingham

Missouri

  • Washington University - St Louis

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2023-03-20
Est. Completion 2026-11-01
Phase NA

Sponsor

University of Alabama at Birmingham

1,160 total trials

What the Registry Record Tells You About NCT05327322

The ClinicalTrials.gov registry entry for NCT05327322 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 199-participant average among 25 other Relapsing Remitting Multiple Sclerosis trials with a reported enrollment target (50% lower). The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Relapsing Remitting Multiple Sclerosis appearing as the primary indexed condition, and to 3 interventions - of which Glycemic load is the first listed.

NCT05327322 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Alabama, Missouri.

Frequently Asked Questions

What is clinical trial NCT05327322 about?

NCT05327322 is a clinical study titled "Functional Outcomes From Diets in Multiple Sclerosis". The purpose of this study is to test the effects of two dietary interventions, glycemic load and calorie restriction, on physical function, cognition, pain, fatigue, mood, and anxiety in adults with multiple sclerosis (MS). The investigators will also explore the how the diet interventions impact in...

What is the current status of trial NCT05327322?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2023-03-20. Estimated completion is 2026-11-01.

What conditions does trial NCT05327322 study?

This clinical trial studies the following conditions: Relapsing Remitting Multiple Sclerosis, Secondary Progressive Multiple Sclerosis.

What interventions are being tested in trial NCT05327322?

The interventions under investigation include: Glycemic load (BEHAVIORAL), Calorie restriction (BEHAVIORAL), Behavioral support (BEHAVIORAL).

Who is sponsoring clinical trial NCT05327322?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05327322 being conducted?

This trial has 2 study locations across Alabama, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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