- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02001402
Chinese Health Investigation of Nurse Aging
November 27, 2013 updated by: Bai Wen-Pei
A follow-up intervention for the climacteric symptoms of nurses in Peking
Study Overview
Status
Unknown
Detailed Description
As we all know,hormone replacement therapy (HRT) is the main therapy to climacteric symptoms.But HRT has also some disadvantages including breast cancer,cardiovascular disease and so on, especially long period of HRT.
It makes us to find the non-hormone therapy.
So we want to investigate the exercise on the effect of climacteric symptoms.Doing exercise is helpful for avoiding and treating many disease,including climacteric symptoms.In our previous research,we found that playing exercise can treat moderate climacteric symptoms.
Study Type
Observational
Enrollment (Anticipated)
2
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
40 years to 55 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
About 2000 nurese aged 40-55 living in peking will be investigated.We will measure the symptoms of perimenopausal syndrome by kupperman index、HRQOL(health -related quality of life) to evaluate the severity of menopausal syndrome and quality of life.We choose nurses whose KMI is above 15 and divided them into intervention group and control group.In intervention group,we give them health education and exercise intervention.
Description
Inclusion Criteria:
- they are nurse ,aged40-55, lived in peking ,who are among perimenopausal women.
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
the number of KMI
Time Frame: up to 2 years
|
KMI is the short of Kupperman index, which is a questionnaire that assesses the severity of women's climacteric symptoms.
|
up to 2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
blood lipid
Time Frame: up to 2 years
|
blood lipid is an index to measure the effect of exercise.
|
up to 2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2008
Primary Completion (Anticipated)
September 1, 2015
Study Completion (Anticipated)
September 1, 2016
Study Registration Dates
First Submitted
November 20, 2013
First Submitted That Met QC Criteria
November 27, 2013
First Posted (Estimate)
December 4, 2013
Study Record Updates
Last Update Posted (Estimate)
December 4, 2013
Last Update Submitted That Met QC Criteria
November 27, 2013
Last Verified
November 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- 83573214
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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