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Genetic Evaluation and Modification of Lifestyles to Improve Female Life Expectancy (GEMLIFE)

Primary Purpose

Menopause Syndrome, Inflammation, Inflammatory Response

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mediterranean diet
AHA walking program
Mindfulness-based stress reduction
Unstructured Mediterranean diet
Unstructured walking program
Unstructured stress reduction
Sponsored by
Rush University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Menopause Syndrome focused on measuring Menopause, Inflammation, Aging, Telomeres, Oxidative Stress, Lifestyle Changes, Mindfulness, Diet, Physical Activity

Eligibility Criteria

40 Years - 60 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Non-hysterectomized women: Amenorrhea > 12 consecutive months Hysterectomized women: Bilateral oophorectomy (3 months after surgery) Normal mammogram in the past year Normal pap smear deemed to be negative within 5 years Able to understand the protocol and sign an informed consent Able to participate in a structured diet program for 12 weeks Able to participate in a structured walking program for 12 weeks Able to participate in a structured mindfulness-stress reduction program Able to operate an I-PAD, and able to connect to the internet Exclusion Criteria: Known or suspected pregnancy Undiagnosed abnormal vaginal bleeding Known or suspected breast cancer or estrogen-dependent neoplasia Known or at risk for a MI, PE or significant cardiovascular event Poorly controlled blood pressure : sitting systolic > 160 or diastolic >95 mmHg Poorly controlled diabetes Uncontrolled thyroid disease Impaired liver function Unstable psychiatric disorder including depression or anxiety, PTSD History of drug or alcohol abuse Treatment with anticoagulants ( heparin, warfarin, lovenox, eliquis) Severe systemic disease which might interfere with interpretation of results Unwilling or unable to follow a diet, exercise or stress reduction protocol

Sites / Locations

  • Rush University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Placebo Comparator

Active Comparator

Placebo Comparator

Arm Label

Intervention group of menopausal women on hormone replacement

Control group of menopausal women on hormone replacement

Intervention group of menopausal women without hormone replacement

Control group of menopausal women without hormone replacement

Arm Description

This group of women on hormone replacement will have specific, structured diet, physical activity, and mindfulness-based stress reduction programs.

This group of women on hormone replacement will be given unstructured guidelines for diet, physical activity, and stress-reduction.

This group of women will have specific, structured diet, physical activity, and mindfulness-based stress reduction programs.

This group of women will be given unstructured guidelines for diet, physical activity, and stress-reduction.

Outcomes

Primary Outcome Measures

Independent Lifestyle Interventions on Telomere Length
Measurement of telomere length after 12 months of a Mediterranean diet, American Heart Association walking program, and mindfulness-based stress reduction program.

Secondary Outcome Measures

Lifestyle Interventions on Inflammatory Biomarkers and Cytokines
Inflammatory biomarkers ( C-Reactive Protein, WBC count) and cytokines (IL-6, TNFa)will be measured before 12 months of Mediterranean diet, the American Heart Association walking program and mindfulness based stress reduction
Measurement of Interventions on Inflammatory Biomarkers and Cytokines
Inflammatory biomarkers C-Reactive Protein, WBC count)after 12 months after a Mediterranean diet, American Heart Association walking program and mindfulness based stress reduction program

Full Information

First Posted
June 21, 2021
Last Updated
February 9, 2023
Sponsor
Rush University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05715372
Brief Title
Genetic Evaluation and Modification of Lifestyles to Improve Female Life Expectancy
Acronym
GEMLIFE
Official Title
Genetic Evaluation and Modification of Lifestyles to Improve Female Life Expectancy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Terminated
Why Stopped
no further funding
Study Start Date
June 22, 2021 (Actual)
Primary Completion Date
June 22, 2021 (Actual)
Study Completion Date
June 22, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rush University Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The GEMLIFE Study is a 12-month clinical trial for menopausal women. The purpose of this study is to promote an improved aging process for women in menopause through lifestyle changes. The changes will include a heart healthy diet, structured walking program, and mindfulness-based stress reduction. During the study, the investigators will monitor components of your genetic make-up that will tell us how you are aging. Investigators will also monitor bloodwork for inflammation that can affect medical conditions. Study participants may qualify if you are within 5 years of your last menstrual period and have well controlled medical conditions. There is no cost to participants to enroll in the study- only potential benefits to the participant's health and aging process.
Detailed Description
The long-term goal of this research is to create and implement lifestyle interventions that will prevent or delay morbidities associated with accelerated aging in the menopausal women. By the end of this year, it is estimated that approximately 50 million women will be in the menopausal phase of their life. Menopause is defined by the decline in estrogen levels and subsequent increase in inflammatory markers which are associated with multiple morbidities involving the brain, bone and cardiovascular systems. Various lifestyle changes have been found to prevent or decrease these morbidities. Hormone replacement therapy in the early years of menopause is also a known therapeutic modality for the treatment of menopausal symptoms. The investigators will evaluate if hormone replacement and lifestyle change will have an enhanced effect on the prevention of morbidity and mortality. Telomeres are distinct structures found at the end of chromosomes. As women enter into menopause, which is the biomarker for aging, there is a shortening of the telomere length. Poor lifestyle factors which cause oxidative stress, can lead to poor cell replication and critical shortening of telomere length. Telomerase, an enzyme which aids in gene sequencing, also declines. Shortened telomere length and low levels of telomerase lead to cell aging and apoptosis, a reduction in normal organ function, and an increase in morbidity and mortality. It has been found that lifestyle intervention, and possibly hormone replacement, can enhance telomere length and telomerase production. This research will focus on the acute menopausal woman (within 5 years of the last menstrual period), with and without hormone replacement, .and multiple lifestyle interventions. Early intervention within the first five years of menopause is most important in affecting long term morbidity and mortality in women. Serial measurement of various biomarkers and cytokines associated with aging, and measurements of telomere length and telomerase levels will be performed over a 9 month period of time. Evidence shows that diet, physical activity and cognitive intervention may synergize when combined in a multimodal intervention as each targets different mechanisms. The Investigators will evaluate the efficacy of each 12-week interventions on telomere length, telomere production, serum biomarkers and cytokine levels before and after each intervention, and as a multimodal approach. Approximately 100 women will be recruited once they have been confirmed to be in the early stages of menopause, then further divided based on the use of hormone replacement. Aims are to: (1) determine the independent and combined efficacies of lifestyle interventions on telomere length, (2) determine the independent and combined efficacies of lifestyle interventions on biomarkers and and cytokines, (3) Determine other mechanisms of aging associated with the acute phase of menopause . This key knowledge will aid in practical and early lifestyle interventions to deter detrimental morbidities in the menopausal women.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Menopause Syndrome, Inflammation, Inflammatory Response, Aging, Menopause, Telomere Shortening, Stress Oxidative
Keywords
Menopause, Inflammation, Aging, Telomeres, Oxidative Stress, Lifestyle Changes, Mindfulness, Diet, Physical Activity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
Randomized, single-blinded prospective study.
Masking
Participant
Masking Description
Computer-assigned.
Allocation
Randomized
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group of menopausal women on hormone replacement
Arm Type
Active Comparator
Arm Description
This group of women on hormone replacement will have specific, structured diet, physical activity, and mindfulness-based stress reduction programs.
Arm Title
Control group of menopausal women on hormone replacement
Arm Type
Placebo Comparator
Arm Description
This group of women on hormone replacement will be given unstructured guidelines for diet, physical activity, and stress-reduction.
Arm Title
Intervention group of menopausal women without hormone replacement
Arm Type
Active Comparator
Arm Description
This group of women will have specific, structured diet, physical activity, and mindfulness-based stress reduction programs.
Arm Title
Control group of menopausal women without hormone replacement
Arm Type
Placebo Comparator
Arm Description
This group of women will be given unstructured guidelines for diet, physical activity, and stress-reduction.
Intervention Type
Behavioral
Intervention Name(s)
Mediterranean diet
Intervention Description
12-week structured program for Mediterranean diet.
Intervention Type
Behavioral
Intervention Name(s)
AHA walking program
Intervention Description
12-week structured AHA walking program.
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness-based stress reduction
Intervention Description
8-week structured mindfulness-based stress reduction (Cabot).
Intervention Type
Behavioral
Intervention Name(s)
Unstructured Mediterranean diet
Intervention Description
Unstructured 12-week program with basic outline for Mediterranean diet.
Intervention Type
Behavioral
Intervention Name(s)
Unstructured walking program
Intervention Description
Unstructured 12-week walking program.
Intervention Type
Behavioral
Intervention Name(s)
Unstructured stress reduction
Intervention Description
Unstructured program using mobile application for stress reduction.
Primary Outcome Measure Information:
Title
Independent Lifestyle Interventions on Telomere Length
Description
Measurement of telomere length after 12 months of a Mediterranean diet, American Heart Association walking program, and mindfulness-based stress reduction program.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Lifestyle Interventions on Inflammatory Biomarkers and Cytokines
Description
Inflammatory biomarkers ( C-Reactive Protein, WBC count) and cytokines (IL-6, TNFa)will be measured before 12 months of Mediterranean diet, the American Heart Association walking program and mindfulness based stress reduction
Time Frame
12 months
Title
Measurement of Interventions on Inflammatory Biomarkers and Cytokines
Description
Inflammatory biomarkers C-Reactive Protein, WBC count)after 12 months after a Mediterranean diet, American Heart Association walking program and mindfulness based stress reduction program
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Measurement of Menopausal aging due to stress and inflammation of the microbiome
Description
Measurement of association between levels of cytokines (IL-6,TNFa)in the microbiome and telomere length
Time Frame
12 months

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Women.
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Non-hysterectomized women: Amenorrhea > 12 consecutive months Hysterectomized women: Bilateral oophorectomy (3 months after surgery) Normal mammogram in the past year Normal pap smear deemed to be negative within 5 years Able to understand the protocol and sign an informed consent Able to participate in a structured diet program for 12 weeks Able to participate in a structured walking program for 12 weeks Able to participate in a structured mindfulness-stress reduction program Able to operate an I-PAD, and able to connect to the internet Exclusion Criteria: Known or suspected pregnancy Undiagnosed abnormal vaginal bleeding Known or suspected breast cancer or estrogen-dependent neoplasia Known or at risk for a MI, PE or significant cardiovascular event Poorly controlled blood pressure : sitting systolic > 160 or diastolic >95 mmHg Poorly controlled diabetes Uncontrolled thyroid disease Impaired liver function Unstable psychiatric disorder including depression or anxiety, PTSD History of drug or alcohol abuse Treatment with anticoagulants ( heparin, warfarin, lovenox, eliquis) Severe systemic disease which might interfere with interpretation of results Unwilling or unable to follow a diet, exercise or stress reduction protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Barbara Soltes, MD
Organizational Affiliation
Rush University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rush University Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://www.rushu.rush.edu
Description
Menopause study website-Gem-Life study
URL
https://www.facebook.com/GEMLIFEStudy
Description
Menopause study social media page

Learn more about this trial

Genetic Evaluation and Modification of Lifestyles to Improve Female Life Expectancy

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