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MenopauseNCT07085078

Progressive Relaxation Exercise, Menopausal Symptoms and Working Performance

A study testing progressive relaxation exercises in people with Menopause and Menopause Related Conditions, run by Aydin Adnan Menderes University at 2 sites in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

Women typically enter menopause between the ages of 40 and 47, and they spend approximately one-third of their lives in this phase. During menopause, many experience hot flashes due to decreased estrogen levels, along with vasomotor changes such as altered heart rhythms and sleep disturbances. Read more about this study

Who is it for?
Ages 45 to 65 years, women onlyHealthy volunteers can take part
Conditions the study is for
Menopause, Menopause Related Conditions
What is being tested?
progressive relaxation exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
106 participants
Where
2 sitesTurkey (Türkiye)
Study dates
30 Apr 2025to 30 Dec 2025
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 to 65 years
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Being a woman between the ages of 45-65
  • Being able to read and understand Turkish
  • Being at least a primary school graduate
  • Not having menstruation for a year

Who cannot join

  • Having a disability in maintaining communication (such as hearing and speaking)
  • Having entered early menopause (no menstruation) through surgery or natural means,
  • Being on hormone therapy
  • Filling out forms incompletely

Trial locations and contacts

2 sites in 1 country.

Turkey (Türkiye)2 sites
  • Bursa Uludag University

    Bursa, 16059

  • Bursa Uludağ Üniversitesi

    Nilufer, Bursa, 16059

Other trials in Turkey (Türkiye)

About this study

Official title: Effects of Progressive Relaxation Exercise on Menopausal Symptoms and Work Performance: A Randomized Control Study

Women typically enter menopause between the ages of 40 and 47, and they spend approximately one-third of their lives in this phase. During menopause, many experience hot flashes due to decreased estrogen levels, along with vasomotor changes such as altered heart rhythms and sleep disturbances. These issues may accompany or occur independently of hot flashes. Additionally, psychological changes can arise, including tension, sudden mood swings, anxiety, stress, and depression. Physiological concerns may include vaginal atrophy and stress incontinence.

Read the detailed description

Previous studies have shown that menopausal symptoms can significantly increase women's social appearance anxiety, depression, stress, and anxiety overall, negatively impacting their quality of life. Moreover, a limited number of recent studies have attempted to explore the relationship between the severity of menopausal symptoms in the workplace and factors such as job performance, career development decisions, and overall work participation.

This study aims to investigate the effects of progressive relaxation exercises on women's menopausal symptoms and their work performance.

Being tested
progressive relaxation exercises
Keywords
menophose, work performance, progressive relaxation, menopausal symptoms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • progressive relaxation exercisesBehavioural

    Participants with menopausal symptoms received progressive relaxation exercise training, led by the responsible researcher who assigned them to the experimental group.

Study groups in NCT07085078
Study groupRoleWhat they receive
EducationExperimentalProgressive relaxation exercis
Receives: Behavioral: progressive relaxation exercises
ControlNo interventionParticipants with menopausal symptoms assigned to the control group will not receive any intervention. They are expected to answer the scale questions used in the study.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Personal information form before intervention

    Evaluation of women using personal information.

    This tool includes questions on women's sociodemographic characteristics

    Measured: Day 1 (During recruitment)

  2. Before intervention, menopausal symptoms

    Evaluation of menopausal symptoms with Menopause Rating Scale (MRS). It is a Likert-type scale consisting of 11 items, including menopausal complaints. For each item, there are options of "0= None", "1= Mild", "2= Moderate", "3= Severe", and "4= Very severe". The lowest possible score is 0, the highest score is 44. An increase in the total score obtained from the scale indicates an increase in the severity of the complaints experienced.

    Measured: Day 1 (during recruitment)

  3. Before intervention, Individual work performance

    Before intervention, participants are evaluated with the "Individual Work Performance Questionnaire"The scale was designed to measure job performance perception. It consists of 18 Likert-type items. A high score on the scale indicates that job performance perception has increased.

    Measured: Day 1 (During recruitment)

Secondary outcomes (2)
  1. After intervention, menopausal symptoms

    Evaluation of menopausal symptoms with Menopause Rating Scale (MRS). (The lowest possible score is 0, the highest score is 44. The increase in the total score obtained from the scale indicates an increase in the severity of the complaints).

    Measured: Ten days after the conclusion of the five-week training program.

  2. After intervention, Individual work performance

    participants are evaluated with the "Individual Work Performance Questionnaire" (The scale was designed to measure job performance perception. It consists of 18 Likert-type items. A high score on the scale indicates that job performance perception has increased.)

    Measured: Ten days after the conclusion of the five-week training program.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Jul 2025
  2. Study start30 Apr 2025
  3. Primary completion30 Sep 2025
  4. Study completion30 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Care provider, Outcomes assessor
Enrolment
106 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07085078
Sponsor's protocol ID
18/17
Status last verified
May 2026
First submitted
26 Jun 2025
Last updated
27 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The responsible researcher will apply the training and exercises and code the data as A and B. A and B will be coded as A and B. The second researcher will apply the question and scale forms coded as A and B. The third researcher will not know which group the A and B data belong to, and the data will be entered into the SPSS program as A and B groups. The analyses will be carried out by the researcher who is blind to the groups. After the analyses are completed, all researchers will know which arm the findings belong to A and B groups. They will be able to access all of the data.

Publications

  • O'Neill MT, Jones V, Reid A. Impact of menopausal symptoms on work and careers: a cross-sectional study. Occup Med (Lond). 2023 Sep 29;73(6):332-338. doi: 10.1093/occmed/kqad078.

    PubMed 37542726
  • Koopmans L, Bernaards CM, Hildebrandt VH, Lerner D, de Vet HC, van der Beek AJ. Cross-cultural adaptation of the Individual Work Performance Questionnaire. Work. 2015;53(3):609-19. doi: 10.3233/WOR-152237.

    PubMed 26835864

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