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New treatment option for Perimenopause
Official title Exercise in Perimenopause to Improve Cognitive Health
ClinicalTrials.gov ID: NCT07272174
What this study is testing
- What it's testing
- Perimenopause is now considered a possible risk factor for dementia and may contribute to the fact that 2/3 of those living with Alzheimer's disease are females. Indeed, research studies show that middle-aged females demonstrate significant declines in their thinking abilities and detrimental changes in their brains as they go through perimenopause.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 40 to 55, women only. Healthy volunteers may be eligible.
You may be able to join if
- Are biological females, as assigned at birth
- Are aged between 40 and 55 years
- Had at least 1 menstrual period in the last 10 months
- Are perimenopausal based on STRAW +10 Staging System, or answer "yes" to MQ6 questions of changes in periods, having hot flashes, or vaginal dryness...
- Have an intact uterus
You likely can't join if
- Are engaged in regular PRT (i.e., 2x/week) in the prior three months
- Are diagnosed with cognitive impairment or dementia of any type
- Are at high risk for cardiac complications during exercise
- Have clinically important peripheral neuropathy or severe musculoskeletal or joint disease that impairs mobility
- Are taking medications that negatively affect cognitive function, such as anticholinergics, major tranquilizers, and anticonvulsants
- Have a BMI \<15 or anorexia nervosa; g) had surgical menopause
See the full eligibility criteria
- Are biological females, as assigned at birth
- Are aged between 40 and 55 years
- Had at least 1 menstrual period in the last 10 months
- Are perimenopausal based on STRAW +10 Staging System, or answer "yes" to MQ6 questions of changes in periods, having hot flashes, or vaginal dryness, pain, or sexual concerns
- Have an intact uterus
- Have a Montreal Cognitive Assessment (MoCA) score \>26/30, indicating normal cognition
- Have subjective cognitive complaints defined as responding "yes" to "Do you feel like your memory or thinking is becoming worse?"
- Completed high school education
- Read and speak English with acceptable visual and auditory acuity
- Are able to safely engage in moderate-intensity PRT as indicated by the PAR-Q+; and
- Are able to provide informed consent.
- Are engaged in regular PRT (i.e., 2x/week) in the prior three months
- Are diagnosed with cognitive impairment or dementia of any type
- Are at high risk for cardiac complications during exercise
- Have clinically important peripheral neuropathy or severe musculoskeletal or joint disease that impairs mobility
- Are taking medications that negatively affect cognitive function, such as anticholinergics, major tranquilizers, and anticonvulsants
- Have a BMI \<15 or anorexia nervosa; g) had surgical menopause
- Had endometrial ablation that resulted in the loss of menstruation
- Have polycystic ovarian syndrome
- Currently undergoing chemo
- Are using estrogen-containing contraception in the last 12 months
- Had premature ovarian failure; or
- Are already enrolled in a drug or exercise trial
The study team makes the final eligibility decision.
Where it's taking place
- Vancouver, British Columbia, Canada
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 40 years to 55 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Vancouver, British Columbia, Canada. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.