Investigating the Impact of Sex Hormones in Multiple Sclerosis

NCT ID: NCT07081594

Last Updated: 2025-07-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

14 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-01

Study Completion Date

2029-03-31

Brief Summary

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Emerging evidence indicates that females with MS experience worsened symptoms during the luteal phase (post ovulation) of the menstrual cycle when progesterone levels rise and estradiol fluctuate. The rapid hormonal swings may disrupt hypothalamic regulation, leading to an increase in body temperature - a well-established trigger for MS symptom exacerbation. These hormonal changes could also affect neuromuscular function, as estradiol and progesterone receptors are present in the nervous system and skeletal muscles.

Three critical aspects of motor rehabilitation are corticospinal excitability, motor learning, and fatigability. Previous research indicates that corticospinal excitability and the capacity to learn fine motor tasks fluctuate across menstrual cycles, indicating hormonal influences on neuroplasticity. However, it remains unclear how these hormonal fluctuations specifically affect corticospinal excitability, motor learning, and motor fatigability in females with MS. Understanding these relationships could significantly improve rehabilitation approaches. For example, pre-menopause females with MS may experience a more optimal state for neuroplasticity during the follicular phase of their cycles, therefore providing a potential window for greater rehabilitation efficacy.

Detailed Description

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The objective of this project is to systematically examine how hormonal fluctuations pre-menopause influence corticospinal excitability, motor learning, and motor fatigability in females with MS. The study is structured around the following specific aims:

Aim 1: Quantify the effects of estradiol and progesterone levels on corticospinal excitability in pre- menopausal females with MS. We will elicit motor evoked potentials by cortical and subcortical stimulation of corticospinal axons using transcranial magnetic stimulation (TMS).

Aim 2: Evaluate how hormonal fluctuations across menstrual phases impact motor learning ability in pre-menopause females with MS. Participants will be asked to perform a finger sequence motor learning task using visual feedback. The task will be performed using a computer keyboard. Participants will be asked to copy the numerical sequence on a monitor in front of them that pertains to a number on the keyboard with their fingers. Participants will be given three different sequences with equivalent difficulty at each session to avoid carry-over effects between visits.

Aim 3: Determine the relationship between hormonal fluctuations and motor fatigability in pre-menopause females with MS. Participants will perform a maximal voluntary force (MVF). Participants will then be asked to pinch to 80% of their MVF, and maintain this hold for as long as possible1. The trial will end when the force drops below 40% MVF. Two trials in total will be performed. Average time to fatigue (40% MVF) and slope of the drop-off will be calculated as a measure of overall fatigue.

Conditions

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Multiple Sclerosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Pre-Menopausal Women

Naturally cycling women with multiple sclerosis

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Age ≥18 years
* Diagnosis of relapsing-remitting, primary progressive or secondary progressive MS with no minimum years since diagnosis
* Stable disease modifying therapies for at least 6 months
* Eumenorrheic females

Exclusion Criteria

* Another diagnosis (e.g., peripheral neuropathies or orthopedic)
* Pregnancy as confirmed by urine test
* Irregular menstrual cycles
* Diagnosis of premenstrual dysphoric disorder or polycystic ovary syndrome
* Taking antipsychotic medications / does not pass the TMS safety checklist
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Milap Sandhu

OTHER

Sponsor Role lead

Responsible Party

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Milap Sandhu

Principle Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Milap Sandhu, PT, PhD

Role: PRINCIPAL_INVESTIGATOR

Shirley Ryan AbilityLab

Central Contacts

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Kailynn Mannella, PhD

Role: CONTACT

312-238-6493

Milap Sandhu, PT, PhD

Role: CONTACT

References

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Christogianni A, O'Garro J, Bibb R, Filtness A, Filingeri D. Heat and cold sensitivity in multiple sclerosis: A patient-centred perspective on triggers, symptoms, and thermal resilience practices. Mult Scler Relat Disord. 2022 Nov;67:104075. doi: 10.1016/j.msard.2022.104075. Epub 2022 Jul 25.

Reference Type BACKGROUND
PMID: 35963205 (View on PubMed)

Karim HT, Huppert TJ, Erickson KI, Wollam ME, Sparto PJ, Sejdic E, VanSwearingen JM. Motor sequence learning-induced neural efficiency in functional brain connectivity. Behav Brain Res. 2017 Feb 15;319:87-95. doi: 10.1016/j.bbr.2016.11.021. Epub 2016 Nov 11.

Reference Type BACKGROUND
PMID: 27845228 (View on PubMed)

Casamento-Moran A, Mooney RA, Chib VS, Celnik PA. Cerebellar Excitability Regulates Physical Fatigue Perception. J Neurosci. 2023 Apr 26;43(17):3094-3106. doi: 10.1523/JNEUROSCI.1406-22.2023. Epub 2023 Mar 13.

Reference Type BACKGROUND
PMID: 36914263 (View on PubMed)

Hackney AC, ed. Sex Hormones, Exercise and Women: Scientific and Clinical Aspects. 1st ed. 2017. Springer International Publishing : Imprint: Springer; 2017. doi:10.1007/978-3-319-44558-81

Reference Type BACKGROUND

Gilli F, DiSano KD, Pachner AR. SeXX Matters in Multiple Sclerosis. Front Neurol. 2020 Jul 3;11:616. doi: 10.3389/fneur.2020.00616. eCollection 2020.

Reference Type BACKGROUND
PMID: 32719651 (View on PubMed)

Other Identifiers

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STU00224323

Identifier Type: -

Identifier Source: org_study_id

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