- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01397318
Effects of Modified TaiChi Exercise on Maternal Stress, Fatigue, Sleep Quality, Biomarkers, and Infant Gestational Age and Birthweight
18. juli 2011 opdateret af: Taipei Medical University WanFang Hospital
Many pregnant women experience stress, fatigue, and poor sleep quality that may influence infant outcomes such as prematurity and low birthweight through immunologic pathway of biomarkers (serum cytokines and c-reactive protein).
In contrast, TaiChi exercise, one kind of physical activity, can increase pulmonary and immune functions and reduce stress may therefore prevent pregnancy complications and further prevent adverse pregnancy outcomes; however, its effects has not been explored in studies.
Therefore, this study aims to investigate relationships between prenatal stress, fatigue, sleep quality, biomarkers, and infant outcomes; modified a TaiChi exercise program suitable for pregnant women; and test the effects of the exercise on reducing stress and fatigue, promote sleep quality, modulate biomarkers, and prevent adverse infant outcomes.
Infant outcomes in the study will be measured with gestational age and birthweight.
The study is a three-stage longitudinal interventional design.
Studieoversigt
Status
Ukendt
Betingelser
Detaljeret beskrivelse
In the first-stage, patterns of prenatal stress, fatigue, and sleep quality will be investigated by surveying 300 pregnant women who are over 23 weeks of gestation and screen for pregnant women with fatigue and poor sleep quality.
In the second-stage, experts in obstetrics and TaiChi will be invited to modify a TaiChi exercise program.
Thirty women who experience fatigue and poor sleep quality will be invited to practice the modified TaiChi exercise.
Comments from those participants on the program will be used to refine the program and a DVD will be made.
After the program is well-designed and recorded, participants recruited for the third-stage study will be randomly assigned to TaiChi or comparison group.
They will be asked to complete questionnaires and give blood samples for biomarker tests when they are at 27-29, 31-33, and 35-37 weeks of gestation; in labor; and at 4-6 weeks postpartum.
In addition to practice the exercise at home, participants in the TaiChi group will practice TaiChi in groups every month.
In contrast, comparison group will be asked to keep on their usual daily activities, no other interventions will be introduced.
Phone calls or postcard will be made or sent routinely to participants to ensure their long-term participation.
Questionnaires used for the study include 10-item Perceived Stress Scale, Multidimensional Assessment of Fatigue Scale, and Pittsburgh Sleep Quality Index.
Descriptive statistics, Pearson correlation, and generalized estimating equations will be applied to understand predictive effects of maternal stress, fatigue, sleep quality, and biomarkers on infant outcomes; and effects of modified TaiChi exercise on maternal stress, fatigue, sleep quality, biomarkers, and infant outcomes.
In addition to develop a modified TaiChi exercise program suitable for pregnant women, the study anticipates that maternal stress, fatigue, and poor sleep quality can predict infant outcomes through immunologic pathway, and the modified TaiChi exercise can reduce maternal stress and fatigue, improve sleep quality, modulate biomarkers, and hence prevent adverse infant outcomes.
Undersøgelsestype
Observationel
Tilmelding (Forventet)
300
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Taipei, Taiwan
- Taipei Medical University-WanFang Hospital
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
17 år og ældre (Barn, Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Prøveudtagningsmetode
Sandsynlighedsprøve
Studiebefolkning
pregnant women
Beskrivelse
Inclusion Criteria:
Criteria for participation are women who:
- are over 17;
- can read Chinese;
- are at or over 24 weeks of gestation;
- pregnant with singleton;
- are not diagnosed of pregnancy complications such as preeclampsia, preterm labor, preterm rupture of membranes, gestational diabetes, and cervical incompetence before recruitment; and
- are willing to complete questionnaires and give blood samples.
Exclusion Criteria:
- pregnant women who do not meet the recruitment criteria will be excluded from the study.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
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Kontrolgruppe
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Forsøgsgruppe
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Szu-Yuan Chou, Taipei Medical University WanFang Hospital
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. september 2010
Studieafslutning (Forventet)
1. juli 2013
Datoer for studieregistrering
Først indsendt
15. juli 2011
Først indsendt, der opfyldte QC-kriterier
18. juli 2011
Først opslået (Skøn)
19. juli 2011
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
19. juli 2011
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
18. juli 2011
Sidst verificeret
1. juli 2011
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 100005
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