Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07401810

Fascial Yoga in Menopausal Women

Aim:

The aim of this study is to evaluate the effects of a structured fascial yoga-based behavioral intervention on perceived stress, cognitive control, and cognitive flexibility in menopausal women. The study aims to determine whether a non-pharmacological and non-invasive behavioral intervention can support psychological and cognitive functioning and reduce perceived stress in menopausal women.

Design:

This study is designed as a randomized controlled, pretest-posttest experimental study with a post-intervention follow-up assessment. Eligible participants will be randomly assigned to either the intervention group or the control group receiving usual care. Outcomes will be assessed at baseline, immediately after the intervention, and at follow-up to evaluate both the immediate and sustained effects of the intervention.

Method:

A total of 60 menopausal women aged 45-65 years will be recruited from the menopause outpatient clinic and randomly assigned to either the intervention group or the control group. The intervention group will participate in a 12-week online fascial yoga program consisting of two 60-minute sessions per week.

In this study, fascial yoga is defined as a fascia-focused, non-pharmacological, and non-invasive behavioral intervention that includes myofascial release techniques, breath regulation, body awareness, and basic yoga practices to support stress regulation and cognitive functioning. The program will include myofascial release techniques, basic yoga postures suitable for all physical fitness levels, and structured breathing exercises. All sessions will be conducted online in a group format, and no audio or video recordings will be taken.

The control group will continue to receive routine outpatient care during the study period. After completion of the follow-up assessments, the fascial yoga program will be offered to participants in the control group upon request.

Data will be collected at three time points: at baseline before the intervention, immediately after completion of the 12-week intervention, and at the follow-up assessment 8 weeks after the intervention. Perceived stress, cognitive control, and cognitive flexibility will be assessed using validated self-report questionnaires.

Hypotheses:

H1: Menopausal women participating in the fascial yoga intervention will show a significant reduction in perceived stress levels compared with the control group at post-intervention and follow-up assessments.

H2: Menopausal women participating in the fascial yoga intervention will show a significant improvement in cognitive control and cognitive flexibility compared with the control group at post-intervention and follow-up assessments.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

45 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female participants aged 45-65 years
  • In the menopausal period, defined as at least 12 months since the last menstrual period
  • Able to read and understand Turkish and to complete self-report questionnaires

Exclusion criteria

  • Current or past diagnosis of a psychiatric disorder or ongoing psychiatric treatment
  • Regular use of antidepressant, anxiolytic, or corticosteroid medications
  • History of cancer or currently receiving active oncological treatment
  • Participation in fascial yoga, yoga, or similar yoga-based programs within the past 6 months
  • Any medical condition that may prevent safe participation in mild physical activity

Treatment and study plan

Fascial Yoga Program

Behavioral

A structured 12-week online fascial yoga program consisting of two 60-minute sessions per week. The intervention focuses on fascial myofascial relaxation, breathing regulation, and body awareness for stress regulation and cognitive functioning. Sessions will be conducted in a group format, and no audio or video recordings will be taken.

Primary outcomes

  1. Perceived Stress Level

    Time frame: Baseline, immediately post-intervention (12 weeks), and 8 weeks post-intervention follow-up

    Change in perceived stress levels measured using the Perceived Stress Scale (PSS-14). The scale consists of 14 items rated on a 5-point Likert scale (0-4), with total scores ranging from 0 to 56. Higher scores indicate higher perceived stress levels.

  2. Cognitive Control and Flexibility

    Time frame: Baseline, immediately post-intervention (12 weeks), and 8 weeks post-intervention follow-up

    Change in cognitive control and cognitive flexibility levels measured using the Cognitive Control and Flexibility Questionnaire. The questionnaire consists of two subscales (cognitive control and cognitive flexibility), with items rated on a 7-point Likert scale. Higher scores indicate better cognitive control and greater cognitive flexibility.

Study contacts

Contact information is provided by the study sponsor or research team.

Ayşe Eminoğlu, RN, MSc, PhD Candidate

CONTACT

[email protected]

+905415998795

Semra Karaca, PhD

CONTACT

[email protected]

+905523050273

Sponsors and collaborators

Lead sponsor

Marmara University

Other

Registry information

Official study title

The Effect of Fascial Yoga on Perceived Stress, Cognitive Control, and Cognitive Flexibility in Menopausal Women

Acronym: FascialYogaM

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Feb 10, 2026
Registry last updated
Jul 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.