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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03989453
Other study ID # University-Jaén
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2019
Est. completion date October 1, 2019

Study information

Verified date September 2021
Source University of Jaén
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To analyze the effects of a Chi Kung exercise program in Spanish menopausal women


Description:

This is a randomized clinical trial of single-blind with 2 arms (Control group and experimental group), in which a pre-treatment-postest design has been used. The study will define two groups: A control group (CG) that will not be submitted to treatment, which will be evaluated in the pre and post phase of the study. Participants assigned to this group will receive general advice on the positive effects of regular physical activity and will be given a guide to recommendations for promoting physical activity. An experimental group (GE) that after an initial evaluation will undergo a physical training program based on Chi Kung exercises. Once the intervention is finished, it will be submitted to a final evaluation to see if there is a difference or not with the results obtained at the beginning.


Recruitment information / eligibility

Status Completed
Enrollment 117
Est. completion date October 1, 2019
Est. primary completion date September 23, 2019
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Cessation of menstrual activity for twelve months or more. - Being able to understand the instructions and exercise protocols of this project Exclusion Criteria: - Contraindications for the performance of physical tests, cancer or serious illness, musculoskeletal and neurological diseases, taking of drugs that affect the central nervous system or antidepressants, or lack of will to participate in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Chi Kung
The duration of the intervention is 12 weeks, with 2 sessions per week of Chi Kung. Each session lasts approximately 1 hour and is structured in three parts: initial warm-up (Based on breathing and concentration exercises), of 10 minutes duration, a 40-45 minute Chi Kung session and finally 10 minutes of guided relaxation.

Locations

Country Name City State
Spain U.E.D. Virgen de la Capilla Jaén

Sponsors (1)

Lead Sponsor Collaborator
University of Jaén

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary PSQI (Pittsburgh Sleep Quality Index) A simple and valid assessment of both sleep quality and disturbance that might affect. They consist of 10 questions divided into four subscales: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep discomfort, medication use and daytime dysfunctions, adding up to a total score. The higher value represents a worse result. At the beginning-at three months
Primary STABILOMETRIC PLATFORM instrument composed of resistive pressure sensors, used to measure the static or postural balance. The test was performed under both eyes-open and eyes-closed conditions At the beginning-at three months
Primary WHQ (The Women's Health Questionnaire) Measures the quality of life related to health specific for menopause At the beginning-at three months
Primary FSFI (The Female Sexual Function Index) Questionnaire that evaluates the sexuality of women during the last four weeks. At the beginning-at three months
Primary MRS (Menopause Rating Scale) Assesses the severity of menopause-related complaints and the impact on health-related quality of life. Calculated by adding up the 11 questions in the questionnaire. Each item has a score of 0-1-2-3-4, with 4 being the worst score. At the beginning-at three months
Primary ABC-16 (Activities Specific Balance Confidence Scale) Questionnaire that assesses balance confidence in performing activities of daily living. It is calculated by adding up the 16 responses of the questionnaire, with 0 being the minimum score and 100 being the maximum score. The higher value represents a better result. At the beginning-at three months
Secondary Handgrip Strength Dynamometer will be employed to assess handgrip strength. At the beginning-at three months.
Secondary HADS (The Hospital Anxiety And Depression) A reliable, valid and practical screening tool for identifying and quantifying anxiety and/or depression in non-patients. At the beginning-at three months.
Secondary SF-36 (The Short Form-36 Health Survey) Used extensively for assessing health-related quality of life. At the beginning-at three months.
Secondary TUG (Timed Up and Go test) Is a simple test used to assess a person's mobility and physical function At the beginning-at three months.
Secondary BMI (Body Mass Index) Is calculated from the formula, Weight (kg) / Height2 (m2), whose unit is kg/m2. It is a rough indicator of total body fat At the beginning-at three months.
Secondary Waist circumference Is used to assess central fat distribution and degree of abdominal obesity. At the beginning-at three months.
Secondary Waist-to-hip ratio Is the dimensionless ratio of the circumference of the waist to that of the hips. This is calculated as waist measurement divided by hip measurement. At the beginning-at three months.
Secondary Cervantes Scale Specific Scale for better quality of life related to specific health for menopause. At the beginning-at three months.
Secondary The Female Genital Self-Image Scale (FGSIS) Scale that evaluates the degree of satisfaction of their own genitals. At the beginning-at three months.
Secondary FSS (Fatigue Severity Scale) A self-report scale describing the severity of fatigue and the impact of fatigue on activities of daily living. At the beginning-at three months.
Secondary FES-I (Falls Efficacy Scale-International) Questionnaire that evaluates the fear of falling. At the beginning-at three months.