Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06599541
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-13
Brief Title:
Efficacy of Hypopressive Exercises Versus Pilates in Women with Abdominal Diastasis in the Postpartum Period a Randomized Controlled Trial
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Efficacy of Hypopressive Exercises Versus Pilates in Women with Abdominal Diastasis in the Postpartum Period a Randomized Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
AD-HE-PI
Brief Summary:
The aim of this study is to compare the effects of two exercise programs in women with abdominal diastasis AD during the postpartum One group will receive hypopressive exercises HE and the other will receive pilates exercise The hypothesis of this study is that the execution of both protocols will offer benefits in the ultrasound values of the AD and in the data collected on the quality of life in the short term and 12 weeks after its completion
Detailed Description:
Objective To compare the efficacy of hypopressive exercises HE versus pilates exercise in women with abdominal diastasis AD during the postpartum and to know the effects of each of the exercises independently
Design Single-blind randomized controlled trial
Setting Faculty of Physical Therapy of Alcalá de Henares UAH
Participants Primiparous women with DA who have vaginal delivery and are in the 3 months postpartum N40
Interventions Participants will be randomly assigned to perform either a HE program focused on freediving work n20 or a pilates program focused on exhalation n20 The intervention will consist of 3 weekly sessions lasting 30 minutes over 12 weeks where they will receive a weekly face-to-face and group session and two home sessions
Main outcome measures The primary outcome will be measurement of the distance between rectus abdominis through ultrasound to be assessed at baseline immediately after the intervention and 12 weeks later The secondary outcome measure will correspond to the measurement of quality of life using the SF-36 Health Questionnaire It will be collected through masked evaluations by 2 physiotherapists at baseline at the end of the intervention and at 12 weeks
Design Single-blind randomized controlled trial
Setting Faculty of Physical Therapy of Alcalá de Henares UAH
Participants Primiparous women with DA who have vaginal delivery and are in the 3 months postpartum N40
Interventions Participants will be randomly assigned to perform either a HE program focused on freediving work n20 or a pilates program focused on exhalation n20 The intervention will consist of 3 weekly sessions lasting 30 minutes over 12 weeks where they will receive a weekly face-to-face and group session and two home sessions
Main outcome measures The primary outcome will be measurement of the distance between rectus abdominis through ultrasound to be assessed at baseline immediately after the intervention and 12 weeks later The secondary outcome measure will correspond to the measurement of quality of life using the SF-36 Health Questionnaire It will be collected through masked evaluations by 2 physiotherapists at baseline at the end of the intervention and at 12 weeks
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None