이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

폐경기 전 운동으로 인지 건강 향상하기 (EPIC)

2026년 10월 16일 업데이트: Teresa Liu-Ambrose, University of British Columbia

갱년기 저항 운동과 인지 건강

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. Thus, perimenopausal females need strategies to bolster their brain health.

The World Health Organization strongly recommends physical activity interventions to reduce the risk of decline in thinking abilities. However, whether exercise can improve thinking abilities and brain health in perimenopausal females has not been examined. Our research aims to address this important knowledge gap in female brain health.

We will study the effects of a 6-month resistance exercise training (e.g., lifting free weights, exercise with weight machine) program on thinking abilities in 50 physically inactive perimenopausal females, aged 40 to 55 years, who are experiencing difficulties with their thinking abilities. In addition to measuring thinking abilities, we will determine if exercise benefits muscle health, heart health, sleep quality, psychological well-being, menopausal symptoms, and quality of life. We will also explore how resistance exercise training improves thinking abilities as such information can lead to new discoveries and therapies for brain health in females.

연구 개요

상세 설명

  1. PURPOSE:

    To determine if progressive resistance training (PRT) can improve cognitive outcomes compared to balance, flexibility, and tone (BAT) exercises in perimenopausal females aged 40-55 years with subjective cognitive complaints.

  2. HYPOTHESIS:

    At the end of the intervention, PRT will result in an increase in words recalled during the RAVLT 20-minute delay vs no improve in BAT.

  3. JUSTIFICATION:

    The menopause transition (MT) negatively impacts cognitive function and the brain. The majority of perimenopausal females experiences cognitive difficulties and have subjective cognitive complaints (SCCs). Verbal episodic memory and processing speed are most negatively impacted by the MT. Cognitive and brain changes during the MT can significantly impact career and financial wellbeing. The MT is thus a critical window to intervene for female brain health. Exercise can reduce dementia risk factors and promote cognitive health. No published randomized controlled trials have examined the effect of exercise on cognitive outcomes in perimenopausal females.

  4. OBJECTIVE:

    To determine if 26 weeks of 2x/week progressive resistance training (PRT) can improve verbal episodic memory performance on the Rey Auditory Verbal Learning Test (RAVLT) compared with balance, flexibility, and tone exercises (BAT) for physically inactive perimenopausal females aged 40-55.

    Optional Qualitative Component: To assess knowledge and experiences of perimenopause (pre- and post-intervention), expectations of exercise intervention (pre-intervention), and perceived benefits of exercise intervention (post-intervention).

  5. RESEARCH DESIGN:

A 26-week, assessor-blinded, two-arm, proof-of-concept trial with 50 physically inactive perimenopausal females, aged 40 to 55 years, with subjective cognitive complaints. Participants will be randomized 1:1 to PRT or BAT and measured at baseline, 13 weeks, and 26 weeks.

연구 유형

중재적

등록 (추정된)

50

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • British Columbia
      • Vancouver, British Columbia, 캐나다, V5Z 1M9
        • 모병
        • University of British Columbia
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

40년 (성인)

건강한 자원 봉사자를 받아들입니다

예

연구 대상 성별

여성

설명

Inclusion 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 for in-person or >=19/22 for telephone , 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.

Exclusion Criteria:

  • 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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 방지
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Progressive Resistance Training (PRT)

Each PRT session will be 1-hr in duration and consists of a warm-up (10 mins), PRT (45 mins), and cool-down (5 mins). 2x/week and group-based.

The sessions will occur in the Exercise Prescription Suite of the Centre for Aging SMART at VCH; this suite is a fully-equipped gym that includes treadmills, bikes, pneumatic resistance training equipment, and free weights. The training stimulus will initially be at 3 sets of 10-15 repetitions with proper form. At week 4, training intensity will progress from 60-82% of predicted 1 repetition maximum (RM) using the 8RM method. Every 4 weeks the 8RM test will be repeated.

다른 이름들:
  • PRT
활성 비교기: Balance, Flexibility, and Tone Exercises (BAT)

Each BAT session will be 1-hr in duration. 2x/week and group-based.

Each BAT session will be 1-hr in duration and consist of Pilates mat exercises, Yoga-based poses and breathing, Kegel exercises, stretches, and relaxation techniques (e.g., visualization).

다른 이름들:
  • 박쥐

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Rey Auditory Verbal Learning Test (RAVLT)
기간: Baseline, 13 weeks, 26 weeks

The RAVLT is a valid, reliable, and widely-used instrument of verbal episodic memory and learning, with normative values.

Baseline, 13 weeks, 26 weeks

2차 결과 측정

결과 측정
측정값 설명
기간
NIH TB Cognitive Battery - Flanker Test
기간: Baseline, 13 weeks, 26 weeks

A measure of executive functions

Baseline, 13 weeks, 26 weeks
NIH TB Cognitive Battery - Dimensional Change Card Sort Test
기간: Baseline, 13 weeks, 26 weeks

A measure of executive functions

Baseline, 13 weeks, 26 weeks
NIH TB Cognitive Battery - Picture Sequence Memory Test
기간: Baseline, 13 weeks, 26 weeks

A measure of visual episodic memory

Baseline, 13 weeks, 26 weeks
NIH TB Cognitive Battery - List Sorting Test
기간: Baseline, 13 weeks, 26 weeks

A measure of working memory

Baseline, 13 weeks, 26 weeks
NIH TB Cognitive Battery - Pattern Comparison Processing Speed Test
기간: Baseline, 13 weeks, 26 weeks

A measure of processing speed

Baseline, 13 weeks, 26 weeks
Everyday Memory Questionnaire
기간: Baseline, 13 weeks, 26 weeks

A subjective measure of memory failure in everyday life

Baseline, 13 weeks, 26 weeks
Muscle strength of quads
기간: Baseline, 13 weeks, 26 weeks

Muscle strength measure by isokinetic dynamometer

Baseline, 13 weeks, 26 weeks
Peripheral QCT of the tibia
기간: Baseline, 13 weeks, 26 weeks

A measure of bone and muscle health

Baseline, 13 weeks, 26 weeks
Blood pressure
기간: Baseline, 13 weeks, 26 weeks

Blood pressure - systolic and diastolic

Baseline, 13 weeks, 26 weeks
Lipid panel
기간: Baseline, 26 weeks

Lipid levels

Baseline, 26 weeks
Hemoglobin A1-C
기간: Baseline, 26 weeks

Average blood sugar levels

Baseline, 26 weeks
C-reactive protein
기간: Baseline, 26 weeks

Measure of inflammation

Baseline, 26 weeks
Health resource utilization
기간: Baseline, 13 weeks, 26 weeks

Cost of health resource used

Baseline, 13 weeks, 26 weeks
Carotid-femoral pulse wave velocity
기간: Baseline, 13 weeks, 26 weeks

Arterial stiffness

Baseline, 13 weeks, 26 weeks
Pittsburgh Sleep Quality Index
기간: Baseline, 13 weeks, 26 weeks

Subjective sleep quality

Baseline, 13 weeks, 26 weeks
Actigraph
기간: Baseline, 13 weeks, 26 weeks

Using actigraphy data, quantify sleep quality (e.g., duration, efficiency, fragmentation).

Baseline, 13 weeks, 26 weeks
Actigraph
기간: Baseline, 13 weeks, 26 weeks

Using actigraphy data, quantify physical activity (e.g., intensity and minutes)

Baseline, 13 weeks, 26 weeks
Actigraph
기간: Baseline, 13 weeks, 26 weeks

Using actigraphy data, quantify sedentary behaviour (minutes)

Baseline, 13 weeks, 26 weeks
Fatigue Severity Scale
기간: Baseline, 13 weeks, 26 weeks

Subjective fatigue

Baseline, 13 weeks, 26 weeks
PHQ-9
기간: Baseline, 13 weeks, 26 weeks

Depression severity

Baseline, 13 weeks, 26 weeks
GAD-7
기간: Baseline, 13 weeks, 26 weeks

Generalized anxiety disorder

Baseline, 13 weeks, 26 weeks
Menopause Rating Scale
기간: Baseline, 13 weeks, 26 weeks

Menopause symptoms

Baseline, 13 weeks, 26 weeks
EuroQol-5 Domain-5 Level
기간: Baseline, 13 weeks, 26 weeks

Quality of life

Baseline, 13 weeks, 26 weeks
International Physical Activity Questionnaire
기간: Every 30 days over 26 weeks

Physical activity

Every 30 days over 26 weeks
DEXA
기간: Baseline, 13 weeks, 26 weeks

Lean mass

Baseline, 13 weeks, 26 weeks
DEXA
기간: Baseline, 13 weeks, 26 weeks

Body fat

Baseline, 13 weeks, 26 weeks
DEXA
기간: Baseline, 13 weeks, 26 weeks

Appendicular Skeletal Muscle Mass Index (ASMI); a measure of sarcopenia

Baseline, 13 weeks, 26 weeks
Mediterranean-DASH Diet Intervention for Neurodegenerative Delay (MIND) Diet score
기간: Baseline, 13 weeks, 26 weeks

Diet

Baseline, 13 weeks, 26 weeks
Processing Speed by smartphone
기간: Baseline, 13 weeks, 26 weeks

Processing Speed

Baseline, 13 weeks, 26 weeks
Memory by smartphone
기간: Baseline, 13 weeks, 26 weeks

Memory

Baseline, 13 weeks, 26 weeks
Productivity Questionnaire
기간: Baseline, 13 weeks, 26 weeks

Measure of work productivity

Baseline, 13 weeks, 26 weeks
Brain-Derived Neurotrophic Factor
기간: Baseline, 26 weeks

Neurotrophic Factor

Baseline, 26 weeks
IGF-1
기간: Baseline, 26 weeks

Neurotrophic Factor

Baseline, 26 weeks
Optional Qualitative Interviews
기간: Baseline, 26 weeks

The interviews will involve questions about participants' experiences and impact of perimenopause in their daily lives, their expectations of an exercise intervention, and perceived benefits of group-based exercise training

Baseline, 26 weeks
Optional Measure: Muscle Health
기간: Baseline, 26 weeks

Myosteatosis measured by Upright Open Magnetic Resonance Imaging (UO-MRI) of the mid-thigh and lower leg (dominant)

Baseline, 26 weeks
Optional Measure: Cerebral Oxygenation
기간: Baseline, 13 weeks, 26 weeks

Measured by the functional near-infrared spectroscopy (fNIRS)

Baseline, 13 weeks, 26 weeks

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Teresa Liu-Ambrose, PhD, University of British Columbia

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 3월 30일

기본 완료 (추정된)

2026년 12월 15일

연구 완료 (추정된)

2027년 1월 30일

연구 등록 날짜

최초 제출

2025년 11월 19일

QC 기준을 충족하는 최초 제출

2025년 11월 26일

처음 게시됨 (실제)

2025년 12월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 20일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 16일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • H25-01552

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다