The Symptom Experience of Women With Perimenstrual Syndrome;Women's Health Related Quality of Life.
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|ClinicalTrials.gov Identifier: NCT00174161|
Recruitment Status : Unknown
Verified July 2005 by National Taiwan University Hospital.
Recruitment status was: Recruiting
First Posted : September 15, 2005
Last Update Posted : September 15, 2005
|Condition or disease||Intervention/treatment|
|Premenstrual Syndrome||Behavioral: self-care, health behavior|
Symptoms are the most common reason people seek health care. Although the menstrual cycle, a normative process, but 10~15% of western women experience sever recurring symptoms associated with the menstrual cycle that can be considered a chronic illness. There are many interventional researches focus on this issue in western countries. There is not only lack of evidence base prevalence of perimenstrual syndrome, but also never found any nursing intervention project focusing on women with perimenstrual syndrome.
The purpose of these series research project is to investigate the prevalence, symptoms cluster and characteristic; establish the systemic symptom management nursing strategies (PMS-SMP); determine short-and long-term effectiveness of PMS-SMP. To enhance the health related quality of life of women with Perimenstrual syndrome. Simultaneously, the PMS-SMP offers a research and clinical based protocol to demonstrate the independent nursing role and practice care model. The 3-year series research process will include three research domains.
Content analysis, descriptive statistics(percentage, mode, medium, quartile, rank), Chi-square, One way ANOVA, MANCOVA, and Step-Wise regression will be applied to examine the research finding. Although focused on perimenstrual symptoms relief and improve the health related quality of life of women with perimenstrual symptoms, these strategies are generally health promoting and can be applied to other women’s health conditions.
|Study Type :||Observational|
|Enrollment :||1000 participants|
|Observational Model:||Defined Population|
|Study Start Date :||August 2005|
|Study Completion Date :||December 2005|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00174161
|Contact: Yang Ya Ling, Master||886-2-23123456 ext firstname.lastname@example.org|
|NTUH, National Taiwan University Hosptal||Recruiting|
|Taipei, 7, Chung-Shan South Road, Taiwan, 100|
|Study Chair:||Yang Ya Ling||National Taiwan University Hospital|