Study to Investigate Effects of a Herbal Drug Compared to Placebo on Sleep
NCT00997256
Dyssomnias, Healthy
Marburg, Hesse, Germany
View Trial DetailsNCT Number: NCT07667699
The goal of this observational study is to learn about the multidimensional determinants of functional health in women aged 45 to 60 years. The study will focus on the role of muscle strength, bone mineral density, body composition, physical activity, sleep quality, depressive symptoms, and menopause-related symptoms in functional health.
The main questions it aims to answer are:
1. Does muscle strength contribute to functional health in women aged 45 to 60 years? 2. Does bone mineral density contribute to functional health in women aged 45 to 60 years? 3. How are physical activity, sleep quality, depressive symptoms, body composition, and menopause-related quality of life associated with functional health?
Participants will:
* Undergo handgrip strength measurement * Perform a 30-second chair stand test * Undergo bone mineral density and body composition assessment * Complete questionnaires about physical activity, sleep quality, depressive symptoms, menopausal symptoms, and quality of life * Provide demographic and clinical information
Trial opening soon.
Get Notified45 year–60 year
Female
Observational
This is a single-center, cross-sectional observational study designed to evaluate the multidimensional determinants of functional health in women aged 45 to 60 years. The study will be conducted at the Department of Obstetrics and Gynecology, Kartal Dr. Lütfi Kırdar City Hospital, Istanbul, Turkey.
Midlife and the menopausal transition are associated with changes in muscle strength, bone mineral density, body composition, metabolic profile, physical performance, sleep quality, mood, and menopause-related symptoms. Functional health is a multidimensional construct encompassing physical capacity, independence in daily activities, psychological well-being, and health-related quality of life. This study will assess functional health using biological, behavioral, psychological, and symptom-related indicators rather than relying on a single test or questionnaire score.
Inclusion criteria
are:
Exclusion criteria
are:
Muscle strength and physical performance will be assessed using handgrip strength measurement with a dynamometer and the 30-second chair stand test. Anthropometric measurements, including body weight and waist circumference, will be obtained. Body composition will be assessed using a bioelectrical impedance analysis device.
Bone health will be evaluated using dual-energy X-ray absorptiometry data. Existing bone mineral density data obtained within the previous 6 months will be used, and no repeat DXA assessment will be carried out. Laboratory parameters include complete blood count, 25-hydroxyvitamin D, vitamin B12, ferritin, liver function tests, lipid profile, glucose-related parameters, HbA1c, and/or HOMA-IR.
Participants will complete validated questionnaires assessing physical activity, vulvovaginal symptoms, menopausal symptoms, menopause-specific quality of life, general health-related quality of life, depressive symptoms, and sleep quality. The questionnaires planned for use include the International Physical Activity Questionnaire-Short Form, Vulvovaginal Symptoms Questionnaire, Menopause Rating Scale, Menopause-Specific Quality of Life Questionnaire-II, SF-36 Health Survey, Beck Depression Inventory, and Pittsburgh Sleep Quality Index.
Data will be collected using standardized case report forms. Questionnaire forms will be provided by the principal investigator and completed by the participants during the study visit. Physical performance tests will be performed in the outpatient clinic by the principal investigator. Body composition measurements will be performed by the co-investigator.
Data quality will be supported by predefined study variables, standardized data-collection forms, and consistency checks during data entry. The database will be reviewed for missing, out-of-range, or inconsistent values. When a variable is unavailable in the medical record, it will be coded as missing. No imputation is planned for unavailable variables; analyses will be conducted using available data, and the number of participants included in each analysis will be reported.
Approximately 200 women are planned for inclusion. This sample size was selected to allow multivariable analyses and structural equation modeling. The planned model is expected to include approximately 15 to 20 observed variables and 20 to 25 free parameters. A minimum sample size of approximately 180 participants was estimated based on the recommended ratio of participants to free parameters in structural equation modeling. Therefore, enrollment of at least 200 participants is planned to improve model stability and allow reliable estimation of model fit indices.
Descriptive statistics will be used to summarize demographic, clinical, functional, densitometric, laboratory, and questionnaire-based variables. Associations between variables will be evaluated using correlation analyses and multivariable regression models. Age, body mass index, menopausal duration, and comorbidities will be considered as covariates. Statistical significance will be set at p < 0.05. Structural equation modeling will be used to examine the structural relationships among muscle health, bone health, body composition, physical activity, sleep quality, depressive symptoms, menopausal symptoms, and functional health.
The study is expected to provide a multidimensional model of functional health in women aged 45 to 60 years and to clarify the independent contribution of muscle and bone health to functional capacity and health-related quality of life during midlife.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
are:
Exclusion criteria
are:
Time frame: Baseline
Functional performance will be operationalised as a composite of two validated measures: (1) number of repetitions completed in the 30-second chair stand test as a measure of lower extremity strength, and (2) dominant hand grip strength (kg) will be measured by calibrated hydraulic hand dynamometer following EWGSOP2 protocol. A standardised composite functional performance z-score will be derived by summing the z-scores of both measures. The primary analysis will examine the independent contributions of bone mineral density and skeletal muscle mass to this composite score using multivariable linear regression and structural equation modelling (SEM).
Time frame: Baseline
Lumbar spine (L1-L4) and Femoral neck areal BMD (g/cm²) will be measured by dual-energy X-ray absorptiometry (DXA). The values will be compared across three age subgroups (45-50, 50-55, 55-60 years).
Time frame: Baseline
Dominant hand grip strength (kg) will be measured by calibrated hydraulic hand dynamometer following EWGSOP2 protocol. Among the three trials performed; mean value will be recorded.
Time frame: Baseline
Number of full sit-to-stand repetitions completed within 30 seconds without arm support, following standardised protocol.
Time frame: Baseline
Total body fat mass (kg) assessed by bioelectrical impedance analysis (BIA).
Time frame: Baseline
Total body fat percentage (%) assessed by bioelectrical impedance analysis (BIA).
Time frame: Baseline
Total fat-free mass (kg) assessed by bioelectrical impedance analysis (BIA).
Time frame: Baseline
Appendicular and total skeletal muscle mass (kg) assessed by bioelectrical impedance analysis (BIA).
Time frame: Baseline
Total body water (litres) assessed by bioelectrical impedance analysis (BIA).
Time frame: Baseline
Body weight (kg) and height (cm) is measured by standardised anthropometry; BMI will be calculated as weight divided by height squared (kg/m²).
Time frame: Baseline
Physical Component Summary (PCS) score derived from the validated Turkish version of the Short Form-36 (SF-36) questionnaire. Score range 0-100; higher scores indicate better physical health-related quality of life.
Time frame: Baseline
Mental Component Summary (MCS) score derived from the validated Turkish version of the SF-36. Score range 0-100; higher scores indicate better mental health-related quality of life.
Time frame: Baseline
Total score from the validated Turkish version of the Menopause-Specific Quality of Life Questionnaire (MENQOL), a 29-item instrument. Score range 1-8 per item; higher scores indicate greater symptom burden across vasomotor, psychosocial, physical, and sexual domains.
Time frame: Baseline
Global PSQI score from the validated Turkish version of the Pittsburgh Sleep Quality Index. Score range 0-21; scores above 5 indicate poor sleep quality.
Time frame: Baseline
Total weekly physical activity expressed as metabolic equivalent of task minutes per week (MET-min/week), calculated from the validated Turkish version of the International Physical Activity Questionnaire - Short Form (IPAQ-SF).
Time frame: Baseline
Fasting venous serum 25-hydroxyvitamin D measured by chemiluminescence immunoassay.
Time frame: Baseline
Fasting venous serum total calcium measured by colorimetric method.
Time frame: Baseline
Fasting venous serum inorganic phosphorus measured by colorimetric method.
Time frame: Baseline
Fasting venous intact PTH measured by electrochemiluminescence immunoassay.
Time frame: Baseline
Fasting venous serum ALP measured as a marker of bone and liver metabolic activity.
Time frame: Baseline
Fasting venous serum osteocalcin measured by immunoassay as a marker of osteoblast activity.
Time frame: Baseline
Venous fasting plasma glucose measured by enzymatic colorimetric method after minimum 8-hour fast.
Time frame: Baseline
HbA1c measured by high-performance liquid chromatography (HPLC) as an index of 3-month glycaemic control.
Time frame: Baseline
Fasting venous serum insulin measured by electrochemiluminescence immunoassay.
Time frame: Baseline
Fasting venous serum total cholesterol measured by enzymatic colorimetric method.
Time frame: Baseline
: Fasting venous serum LDL cholesterol measured by direct homogeneous assay
Time frame: Baseline
Fasting venous serum HDL cholesterol measured by direct homogeneous assay.
Time frame: Baseline
Fasting venous serum triglycerides measured by enzymatic colorimetric method after minimum 8-hour fast.
Time frame: Baseline
Fasting venous serum FSH measured by electrochemiluminescence immunoassay as an endocrine indicator of menopausal transition stage.
Time frame: Baseline
Fasting venous serum estradiol measured by electrochemiluminescence immunoassay.
Contact information is provided by the study sponsor or research team.
Kartal City Hospital
Other
Multidimensional Determinants and Structural Foundations of Functional Health In Women Aged 45-60: The Role of Muscle and Bone Health
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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.
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