Hormone thERapy Effects on BRAin-HEART Health During the Menopausal Transition (HERBRAVEHEART)
HER BRAVE HEART Trial - Hormone thERapy Effects on BRAin-HEART Health During the Menopausal Transition: A Randomized Feasibility Study
The goal of this clinical trial is to learn whether it is feasible to conduct a larger study comparing transdermal menopausal hormone therapy (MHT) versus no hormone therapy in menopausal women with vasomotor symptoms (hot flashes and night sweats) and at least one cardiovascular risk factor. The main questions it aims to answer are:
- What proportion of eligible women agree to be randomly assigned to either receive MHT or not?
- How many participants complete the 12-month follow-up, including repeat heart imaging?
- Does transdermal MHT affect early changes in heart muscle tissue as measured by cardiac MRI?
Researchers will compare immediate initiation of transdermal estradiol (a skin gel or patch) to a no-hormone therapy strategy to see if MHT influences early cardiovascular and brain-vascular changes over 12 months.
Participants will:
- Be randomly assigned to start transdermal MHT within 2 weeks, or to use no hormone therapy for at least the first 3 months
- Undergo a cardiac MRI and retinal eye imaging at the start of the study and again at 12 months
- Complete cognitive testing and questionnaires about symptoms, sleep, and stress at both visits
- Provide a blood sample for storage and future analysis of heart and brain health markers
- Receive follow-up phone calls at 3, 6, and 9 months to review symptoms, medications, and any health changes
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 4
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Amytis HEIM, MD
- Telefonnummer: 12633813556
- E-mail: amytis.heim@mail.mcgill.ca
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Women aged ≥ 45 years.
Perimenopausal or postmenopausal, defined as at least one of the following:
- Perimenopause, defined as menstrual cycle irregularity (changes in cycle length, skipped cycles, or amenorrhea ≥ 60 days) accompanied by vasomotor symptoms consistent with the menopausal transition.
Postmenopause, defined as at least one of:
- ≥ 12 months of spontaneous amenorrhea, or
- bilateral oophorectomy, or
- hysterectomy with FSH > 40 IU/L when menstrual history is unavailable.
Vasomotor symptoms with a negative impact on quality of life, defined as :
- Recurrent hot flashes (sudden sensations of heat, typically involving the face, neck, or chest, often associated with flushing and/or sweating), and/or
- Night sweats (episodes of excessive sweating during sleep), With associated interference in daily functioning, sleep, or overall quality of life, such that the participant would be an appropriate candidate for systemic menopausal hormone therapy in clinical practice.
Presence of at least one cardiovascular risk factor, defined as either:
- Hypertension (diagnosed hypertension, use of antihypertensive medication, or blood pressure ≥ 140/90 mmHg on screening).
- Dyslipidemia (diagnosed dyslipidemia, use of lipid-lowering therapy, LDL ≥ 3.0 mmol/L, or total cholesterol ≥ 5.2 mmol/L).
- Type 2 diabetes mellitus, defined as HbA1c ≥ 6.5%, fasting plasma glucose ≥ 7.0 mmol/L, or use of glucose-lowering medication.
- Obesity (body mass index ≥ 30 kg/m²).
- Current smoking.
- First-degree family history of premature cardiovascular disease, defined as myocardial infarction, stroke, or documented coronary artery disease occurring before age 55 years in a male relative or before age 65 years in a female relative.
- Eligible for systemic MHT (i.e., no formal contraindication to MHT).
- Able and willing to undergo research CMR and attend the 12-month follow-up assessment.
- Able to provide written informed consent.
- Not currently using systemic MHT at baseline, or willing to discontinue systemic MHT prior to randomization and remain off systemic MHT until allocation and baseline assessments are complete.
Exclusion Criteria:
- Prior cardiovascular event or established cardiovascular disease, including myocardial infarction, stroke or TIA, coronary artery disease, heart failure, cardiomyopathy, or clinically significant valvular heart disease.
- Uncontrolled hypertension or other unstable cardiovascular condition (e.g., unstable angina, decompensated heart failure, uncontrolled arrhythmia).
- Formal contraindication to systemic menopausal hormone therapy, including estrogen-dependent cancer, unexplained vaginal bleeding, active severe liver disease, severe thrombophilia, antiphospholipid syndrome, prior or active VTE.
- Standard contraindications to MRI (e.g., MRI-incompatible pacemakers or intracardiac devices, certain metallic implants, metallic foreign bodies in the eye, or severe claustrophobia not manageable).
- Pregnant.
- Active cancer on ongoing cardiotoxic chemotherapy.
- Current use of systemic hormonal therapy outside the study strategy, including systemic menopausal hormone therapy, combined hormonal contraception, or systemic progestin-only contraception, with unwillingness or inability to discontinue prior to baseline and randomization.
- Ten years or more since menopause, defined as ≥10 years from the final menstrual period or from bilateral oophorectomy
- Participants currently using combined hormonal contraception or systemic progestin-only contraception who are willing to discontinue must complete a washout period of at least 4 weeks prior to the baseline visit and randomization
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Aktiv komparator: Non Hormonal Management of Vasomotor Symptoms
Non hormonal management of vasomotor symptoms
|
Participants randomized to this arm will not initiate systemic menopausal hormone therapy for at least the first 3 months following randomization.
Non-hormonal management of vasomotor symptoms is permitted at the discretion of the treating physician, and may include lifestyle interventions, supplements, and/or guideline-recommended non-hormonal pharmacologic therapies such as SSRIs/SNRIs, gabapentin, oxybutynin, or fezolinetant.
If participants experience persistent or intolerable vasomotor symptoms despite non-hormonal management, initiation of systemic MHT may be proposed after 3 months based on shared decision-making between the participant and her treating physician.
All crossovers will be documented including timing, reason, and regimen.
Participants will remain analyzed in their originally assigned group for intention-to-treat analyses.
Andre navne:
|
|
Eksperimentel: Transdermal Menopausal Hormone Therapy
|
Participants randomized to this arm will initiate systemic transdermal estradiol within 2 weeks of the baseline visit. The specific formulation and dose will be selected through shared decision-making between the participant and her physician based on individual clinical factors, tolerability, and patient preference. Permitted formulations include: Estrogel® (0.06% estradiol gel): 1 pump (0.75 mg) to 2 pumps (1.5 mg) applied daily Divigel® (0.1% estradiol gel): 1.0 mg sachet applied once daily Estradot® (estradiol patch): 25, 37.5, or 50 mcg, changed twice weekly Climara® (estradiol patch): 25, 37.5, or 50 mcg, changed once weekly Participants with a uterus will receive endometrial protection. First-line therapy is micronized progesterone (Prometrium® 100 mg orally once daily, continuous regimen). Alternative progestogens (medroxyprogesterone acetate 2.5 mg orally once daily or a levonorgestrel-releasing intrauterine device) may be used if clinically indicated or not tolerated. Dose ad
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Recruitment Rate
Tidsramme: At enrollment
|
Proportion of eligible women approached who consent to randomization, Percentage (%)
|
At enrollment
|
|
12-Month Retention Rate
Tidsramme: 12 months
|
Proportion of randomized participants completing the 12-month follow-up visit, Percentage (%)
|
12 months
|
|
CMR Completion Rate
Tidsramme: 12 months
|
Proportion of participants completing both baseline and 12-month CMR examinations, Percentage (%)
|
12 months
|
|
Crossover Rate
Tidsramme: 12 months
|
Proportion of participants in the no-MHT group who initiate systemic MHT during follow-up, Percentage (%)
|
12 months
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Myocardial oxygenation reserve
Tidsramme: Baseline and 12 months
|
Percent change in myocardial signal intensity (ΔSI%) during breath-hold at 30 seconds relative to rest, assessed by OS-CMR (B-MORE)
|
Baseline and 12 months
|
|
Aortic distensibility
Tidsramme: Baseline and 12 months
|
assessed by CMR, mmHg-¹
|
Baseline and 12 months
|
|
Aortic cross-sectional area
Tidsramme: Baseline and 12 months
|
assessed by CMR, cm²
|
Baseline and 12 months
|
|
Left ventricular ejection fraction (LVEF)
Tidsramme: Baseline and 12 months
|
Assessed by CMR, Percentage (%)
|
Baseline and 12 months
|
|
Left ventricular end-diastolic volume (LVEDV)
Tidsramme: Baseline and 12 months
|
Assessed by CMR, mL
|
Baseline and 12 months
|
|
Left ventricular end-systolic volume (LVESV)
Tidsramme: Baseline and 12 months
|
Assessed by CMR, mL
|
Baseline and 12 months
|
|
Left ventricular mass (LVM)
Tidsramme: Baseline and 12 months
|
Assessed by CMR, grams (g)
|
Baseline and 12 months
|
|
LV mass-to-volume ratio (concentricity)
Tidsramme: Baseline and 12 months
|
Assessed by CMR, g/mL
|
Baseline and 12 months
|
|
Global longitudinal strain (GLS)
Tidsramme: Baseline and 12 months
|
Assessed by CMR, Percentage (%)
|
Baseline and 12 months
|
|
Superficial retinal capillary plexus vessel density
Tidsramme: Baseline and 12 months
|
Assessed by OCT-A, Percentage (%)
|
Baseline and 12 months
|
|
Deep retinal capillary plexus vessel density
Tidsramme: Baseline and 12 months
|
Assessed by OCT-A, Percentage (%)
|
Baseline and 12 months
|
|
Foveal avascular zone (FAZ) area
Tidsramme: Baseline and 12 months
|
Assessed by OCT-A, mm2
|
Baseline and 12 months
|
|
FAZ perimeter
Tidsramme: Baseline and 12 months
|
Assessed by OCT-A, mm
|
Baseline and 12 months
|
|
PROMIS Cognitive Function Short Form 8a score
Tidsramme: Baseline and 12 months
|
Patient-reported cognitive function; scores range 8-40, higher scores indicate better cognitive function
|
Baseline and 12 months
|
|
RBANS Total Scale Score
Tidsramme: Baseline and 12 months
|
Objective neuropsychological assessment of global cognitive function; standardized score (mean 100, SD 15), higher scores indicate better performance
|
Baseline and 12 months
|
|
Global native myocardial T1 according to vasomotor symptom burden
Tidsramme: Baseline
|
Baseline native T1 (ms) assessed by CMR, compared between women with high vs. low vasomotor symptom burden at baseline, defined by HFRDIS score
|
Baseline
|
|
LVEF according to vasomotor symptom burden
Tidsramme: Baseline
|
Baseline LVEF assessed by CMR, compared between women with high vs. low vasomotor symptom burden at baseline, defined by HFRDIS score, Percentage (%)
|
Baseline
|
|
Multivariable regression analysis of baseline predictors of 12-month change in global native myocardial T1
Tidsramme: Baseline and 12 months
|
Exploratory multivariable linear regression will be used to identify associations between baseline clinical, lifestyle, and menopause-related factors (including age, BMI, blood pressure, lipid levels, smoking status, time since menopause, and vasomotor symptom burden) and 12-month change in global native myocardial T1 assessed by CMR.
This analysis aims to identify candidate predictors for future cardiovascular risk stratification.
The dependent variable is change in global native T1 (ms) from baseline to 12 months.
|
Baseline and 12 months
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Hormoner
- Hormoner, hormonsubstitutter og hormonantagonister
- Neurotransmittermidler
- Membrantransportmodulatorer
- Neurotransmitter optagelseshæmmere
- Serotoninmidler
- Aminosyrer, peptider og proteiner
- Organiske kemikalier
- Farmaceutiske præparater
- Doseringsformer
- Farmakologiske handlinger
- Kemiske handlinger og anvendelser
- Kulbrinter
- Cyclohexanes
- Cycloparaffiner
- Kulbrinter, alicyklisk
- Kulbrinter, cyklisk
- Syrer, acyklisk
- Carboxylsyrer
- Polycykliske forbindelser
- Aminer
- Aminosyrer
- Steroider
- SMUSED-RING-forbindelser
- Estrenes
- Estraner
- Estradiol kongenere
- Gonadale steroidhormoner
- Gonadale hormoner
- Gamma-Aminobutyric Acid
- Aminobutyrater
- Butyrater
- Komplekse blandinger
- Syrer, carbocykliske
- Kolloider
- Cyclohexanecarboxylsyrer
- Gabapentin
- Østradiol
- Selektive Serotonin-genoptagelseshæmmere
- Fezolinetant
- Geler
- oxybutynin
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- MP-37-2026-12489
Plan for individuelle deltagerdata (IPD)
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