Ignite Creation Date:
2024-05-06 @ 5:54 PM
Last Modification Date:
2024-10-26 @ 2:38 PM
Study NCT ID:
NCT05474248
Status:
UNKNOWN
Last Update Posted:
2022-07-26
First Post:
2022-07-22
Brief Title:
Diaphragmatic Breathing Training on Postpartum Anxiety
Sponsor:
Ministry of Science and Technology Taiwan
Organization:
Ministry of Science and Technology Taiwan
Study Overview
Official Title:
Effects of A Biofeedback-assisted Diaphragmatic Breathing Training on Postpartum Anxiety A Randomized Controlled Trial
Status:
UNKNOWN
Status Verified Date:
2022-07
Last Known Status:
ENROLLING_BY_INVITATION
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This is a two-group pretest-posttest triple-blinded and randomized controlled trial examining the effects of a biofeedback-assisted diaphragmatic breathing training on postpartum anxiety This study will include full-term postpartum women aged from 20 to 49 who experienced anxious symptoms with State Anxiety Inventory A-State scored 40 or more at the first postpartum day Participants will be randomly assigned to either an experimental group n 64 or a control group n 64 The experimental group will undergo the diaphragmatic breathing training assisted with StressEraser to breath slowly 4-6 times per minute and practice 15 minutes twice daily Participants in the control condition receive postpartum usual care The outcome measures include anxiety measured by State-Trait Anxiety Inventory STAI and the physiological parameters expressed by blood pressure BP and heart rate HR Measurements will be taken at the first postpartum day and one month postpartum We except this breathing training design is able to improve womens postpartum anxiety and in turn improve their physio-psychological health breastfeeding and baby care skills
Detailed Description:
Ditto
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None