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Clinical Trials in Spain / NCT07346703
Enrolling by invitation Not applicable

Effects of DHA in Patients With Multiple Sclerosis

NCT07346703 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-01
Last updated
2026-01-16

Condition(s) studied

Multiple SclerosisPerformance EnhancementSupplemental Nutrition Assistance Program EducationStrength OutcomesFunction ImprovementIntervention Study

Investigational drug(s) / intervention(s)

Docosahexaenoic Acid (DHA) Dietary SupplementDocosahexaenoic Acid (DHA) Dietary SupplementSunflower OilSunflower Oil

Docosahexaenoic Acid (DHA) Dietary Supplement: Subjects will take 2 g of DHA per day for 3 months.

Docosahexaenoic Acid (DHA) Dietary Supplement: Subjects will take 2 g of DHA per day + therapeutic exercise (3 times a week) for 3 months.

Sunflower Oil: Subjects will take 2 g of placebo (sunflower oil) per day for 3 months.

Sunflower Oil: Subjects will take 2 g of placebo per day + therapeutic exercise (3 times a week) for 3 months.

Study summary

This clinical trial will investigate the effects of combining therapeutic exercise with DHA supplementation in 100 patients with multiple sclerosis using a randomized controlled design. Participants, diagnosed according to the McDonald criteria, will undergo functional, cognitive, fatigue, and quality-of-life assessments through tools such as the EDSS, BRB-N, MFIS, EVA-f, and MSQoL-54. Physiological evaluations will include infrared thermography, isokinetic strength testing, perceived exertion (Modified Borg Scale), balance (Timed Up and Go), lower-limb power (Sit-to-Stand app), and handgrip strength. The study hypothesizes that this combined intervention will improve motor function, cognition, fatigue management, and overall quality of life by enhancing neuromuscular activation and metabolic efficiency.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: The patient sample comes from the Multiple Sclerosis Association (AMDEM) of the Murcia region and the neurology department of the Ribera Salud Hospital in Molina de Segura. Patients diagnosed with multiple sclerosis according to the McDonald criteria, aged between 18 and 65 (approximately), who have not suffered any flare-ups in the previous month and who have a score of 0.00 to 6 on the Expanded Disability Status Scale (EDSS) and are able to activate the tibialis anterior muscle will be eligible for the study. Exclusion Criteria: * Not fulfilling the inclusion criteria. * Having any problems performing the tests. * Having any problems taking the supplement or placebo.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Research Center for High Performance Sport. Universidad Católica de Murcia La Ñora Murcia

More Francisco Javier Martínez Noguera trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07346703 on ClinicalTrials.gov ↗ ← All trials in Spain