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A Pilot Study to Evaluate the Effects of Lifestyle Medicine and Mindfulness-based Group Medical Visits on Stress, Microbiome, and Quality of Life in Women Experiencing Perimenopause and Menopause

27 maggio 2026 aggiornato da: Beth Steinberg, Ohio State University

While perimenopause and menopause are natural biological transitions, women may experience a wide range of physical, emotional, and cognitive symptoms. Although pharmacological options for symptom relief are available, these options may not be acceptable or suitable for all women. Integrative approaches for symptom relief, offered through group medical visits, may complement traditional therapies by increasing access to providers, allowing more time for focused education, and fostering supportive discussions with other women experiencing similar symptoms of perimenopause or menopause.

The purpose of this study is to assess the effectiveness of eight monthly group medical visits that incorporate individual physical assessments, focused education on the foundational elements of Lifestyle Medicine relative to health and well-being, mindfulness practices, and community-building discussions with women experiencing perimenopause or menopause. Individual outcomes, obtained before the group medical visits begin, at each monthly group medical visit, and four months after the group medical visits are completed, will include measures of your perimenopause or menopause symptoms, stress, inflammation, microbiome (good bacteria in the body), height/weight, body mass index (BMI), systolic and diastolic blood pressure, and self-reported perceptions of physical, mental, and social health.

Each 120-minute monthly group medical visit, led by a specially trained nurse practitioner and a mindfulness instructor, will include a brief physical assessment, educational discussions related to menopause and lifestyle medicine, experiential mindfulness practices, and the development of individual health and well-being goals.

Panoramica dello studio

Stato

Non ancora reclutamento

Descrizione dettagliata

Group Medical Visits (GMVs), also known as Shared Medical Appointments (SMAs), were introduced in literature in the 1970s, and despite support from organizations such as the American Academy of Family Physicians they have been slow to gain traction in the healthcare field. GMVs provide benefits to patients including increased access and time with the provider, improved quality of care, nonpharmacologic treatment, and the ability to share self-management tools. There is evidence that the GMV experience may impact clinical outcomes in patients with various diseases and conditions such as chronic pain, diabetes, breast cancer, and Multiple Sclerosis. However, the effects of GMVs on clinical and non-clinical outcomes for women - particularly for female-specific conditions like menopause - are not well established.

There is a clear demand for innovative and accessible care models like GMVs to address gaps in menopause care for women. More recently, a number of women are opting out of hormone therapy for menopause and exploring more integrative, holistic approaches to healthcare. Alternative approaches may include Lifestyle Medicine (LM) and mindfulness-based practices. Studies have demonstrated that mindfulness strategies, like meditation or yoga, can be a beneficial component to GMVs. Lifestyle Medicine, as defined by American College of Lifestyle Medicine (ACLM) is a "medical specialty that uses therapeutic lifestyle interventions as a primary modality to treat chronic conditions including, but not limited to, cardiovascular diseases, type 2 diabetes, and obesity". When applied intensively, Lifestyle Medicine has even been shown to reverse chronic conditions. Furthermore, Lifestyle Medicine interventions based on diet, physical activity and sleep hygiene have been shown to improve cardiometabolic outcomes. These types of choices for menopause interventions need support from knowledgeable providers of integrative techniques.

In addition to lifestyle and mindfulness-based interventions, investigating physiological factors in stress such as the microbiome offers a more comprehensive view of health during menopause. The gut microbiome, which consists of the ecosystem of microorganisms inhabiting the gastrointestinal tract, is known to undergo significant changes with aging and menopause. As the gut microbiome plays a key role in psychological stress and overall health, a better understanding of the changes taking place in the microbiome during menopause will help identify areas for improvement and potential interventions for women during this transition.

The aim of this pilot study is to investigate the measurable effects of Lifestyle Medicine GMVs and mindfulness on stress, microbiome, and quality of life in women experiencing perimenopause and menopause. It is anticipated that the GMVs and mindfulness techniques will provide beneficial outcomes for the patients participating in the study, including a reduction of stress, inflammation, BMI, blood pressure and an increase in resilience. Additionally, we anticipate positive trends in self-reported perceptions of health such as physical, mental, and social quality of life. Potential challenges, risks or pitfalls of the study include recruiting a diverse patient population, self-reported data are subject to bias, and the billing structure for GMVs.

This research is significant to women experiencing peri- and post-menopause as it will provide data for future studies to implement more effective, engaging models for managing their health and well-being. Provider-patient contact time has decreased over the years, which can lead to poor health outcomes for patients. GMVs facilitate group healthcare without sacrificing personalization, patient education, and clinical components such as measuring vitals. The implications on a societal level are potential outcomes such as increased access to patient-centered, integrative healthcare, as well as customized non-pharmacological treatment for menopausal women. GMVs provide, or augment, solutions for women who elect not to take hormonal therapy for menopause symptoms. This GMV for the menopausal population will be called Navigating Menopause with a Mindfulness-Based Group Medical Visit.

Tipo di studio

Interventistico

Iscrizione (Stimato)

40

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Ohio
      • Columbus, Ohio, Stati Uniti, 43210
        • The Ohio State University
        • Contatto:
        • Contatto:
        • Sub-investigatore:
          • Beth Steinberg, PhD, RN

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Biological female.
  2. Age 40 to 60.
  3. Irregular menstruation for 3 months and experiencing perimenopause or menopause as determined by reporting at least one symptom on the Menopause Quality of Life Questionnaire (MENQOL).
  4. Ability to attend group medical visits monthly, in-person for 8 months, at The Ohio State University Center for Integrative Health as well as the baseline and end of study visit.
  5. Ability to participate in the Mindfulness in Motion (MIM) study activities.
  6. Ability and willingness to download MyCap, the smartphone app that securely links participant study responses to the REDCap study project.
  7. WiFi connectivity or LTE to allow use of MyCap when not at OSU study site

Exclusion Criteria:

  1. Participants with surgically induced menopause, e.g., hysterectomy, oophorectomy.
  2. Currently receiving or planning to receive hormone therapy for perimenopausal or menopausal symptoms.
  3. Currently taking or planning to take hormonal contraceptives.
  4. Currently taking or planning to take hormone altering medications; i.e. Taxol.
  5. Currently taking probiotics, Siberian rhubarb (Rheum rhaponticum), Black cohosh (Actaea racemosa), Chaste tree berry (Vitex agnus-castus).
  6. Inability to read and/or understand English (consent and questionnaires in English).
  7. Current severe alcohol or substance abuse disorder.
  8. Participants with documented cognitive disorder that limits the ability to independently read, understand, and/or complete the survey or biological; i.e. dementia, Alzheimer's or biological tests.
  9. Participants with major psychiatric disorders not controlled by medication or other psychiatric treatments.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Terapia di supporto
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Intervention Group
Research subjects will participate in eight monthly group medical visits that incorporate individual physical assessments, focused education on the foundational elements of Lifestyle Medicine relative to health and well-being, mindfulness practices, and community-building discussions with women experiencing perimenopause or menopause. Each group medical visit will be 120 minutes in length.

Over the course of eight months, the group medical visits will incorporate individual physical assessments, focused education on the foundational elements of Lifestyle Medicine relative to health and well-being, mindfulness practices, and community-building discussions with women experiencing perimenopause or menopause. Each group medical visit will be 120 minutes in length and will include:

  1. Check-in/physical assessment/self-report surveys (15 min)
  2. Education/Lifestyle Medicine session (30-45 min)
  3. Mindfulness in Motion (MIM) (30 min)
  4. Goals/Questions and 1:1 visits as needed (30 min)

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Blood Pressure
Lasso di tempo: From enrollment to the end of the 12-month study period.
Blood pressure is the force exerted by circulating blood against the walls of blood vessels due to heart's pumping action. It is measured in mmHg. The upper number is the measurement during the heartbeat (systolic) and the lower number is while the heart is at rest (diastolic).
From enrollment to the end of the 12-month study period.
Body Mass Index
Lasso di tempo: From enrollment to the end of the 12-month study period
An indirect measure of body fat derived by dividing weight in kilograms by height in meters, squared.
From enrollment to the end of the 12-month study period

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Salivary Alpha Amylase
Lasso di tempo: From enrollment to the end of the 12-month study period.
Salivary α-amylase is a surrogate marker of sympathetic nervous system activity.
From enrollment to the end of the 12-month study period.
High sensitivity C-Reactive Protein (hs-CRP)
Lasso di tempo: From enrollment to the end of the 12-month study period.
A measure of a protein produced in the liver in response to inflammation, injury or infection.
From enrollment to the end of the 12-month study period.
Perceived Stress Scale
Lasso di tempo: From enrollment to the end of the 12-month study period.
A self-report measure for assessing how unpredictable, uncontrollable, and overwhelming individuals perceive their lives.
From enrollment to the end of the 12-month study period.
PROMIS-29 V2.0
Lasso di tempo: From enrollment to the end of the 12-month study period.
A comprehensive self-report health assessment tool used to assess functioning and well-being. It assesses seven health domains (physical function, fatigue, pain interference, depressive symptoms, anxiety, ability to participate in social activity and sleep disturbance plus a pain intensity rating).
From enrollment to the end of the 12-month study period.
The Menopause-specific Quality of Life Questionnaire
Lasso di tempo: From enrollment to the end of the 12-month study period.
A 29-item self-report tool that assesses the impact of menopausal symptoms over the past month on health-related quality of life in the immediate post-menopausal period.
From enrollment to the end of the 12-month study period.
The Menstrual Distress Questionnaire
Lasso di tempo: From enrollment to the end of the 12-month study period.
A self-report tool designed to comprehensively assess menstrual-related distress. It includes 25 items covering symptoms such as pain, cognitive changes, and gastrointestinal issues, evaluating their impact on functioning, quality of life, and frequency.
From enrollment to the end of the 12-month study period.
Physical Activity Vital Sign
Lasso di tempo: From enrollment to the end of the 12-month study period.
A self-report two question assessment designed to gage physical activity over past week (question 1) and over a typical week (questions 2).
From enrollment to the end of the 12-month study period.

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Vaginal Microbiome Analysis
Lasso di tempo: From enrollment to the end of the 12-month study period.
16S ribosomal RNA sequencing analysis will be used to analyze vaginal secretions to determine microbial diversity, particularly assessing tryptophan since it has been shown to correlate with estrogen regulation.
From enrollment to the end of the 12-month study period.
Rectal Microbiome Analysis
Lasso di tempo: From enrollment to end of the 12-month study period.
Fecal matter will be assessed using 16S ribosomal RNA sequencing to determine microbial diversity, particularly looking at tryptophan metabolism since it has been shown to correlate with estrogen regulation.
From enrollment to end of the 12-month study period.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 agosto 2026

Completamento primario (Stimato)

1 ottobre 2027

Completamento dello studio (Stimato)

30 agosto 2028

Date di iscrizione allo studio

Primo inviato

27 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

27 maggio 2026

Primo Inserito (Effettivo)

2 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

2 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 20260389

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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