Ignite Creation Date:
2024-06-16 @ 11:47 AM
Last Modification Date:
2024-10-26 @ 3:30 PM
Study NCT ID:
NCT06420635
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-05-30
First Post:
2024-05-14
Brief Title:
Maternal Self-efficacy and Motor Development in Premature Infants Clinical Trial Protocol
Sponsor:
Universidad de la Sabana
Organization:
Universidad de la Sabana
Study Overview
Official Title:
Effect of an Interdisciplinary Intervention Program on Maternal Self-efficacy and Motor Development of Premature Children Clinical Trial Protocol
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
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:
Mothers of premature newborns face special home care situations due to the conditions of their children after hospital discharge This requires promoting the positive perception of maternal self-efficacy and thus achieving the reinforcement of behaviors related to the demand for care in relation to motor development
Objective Determine the effect of an interdisciplinary intervention program on maternal self-efficacy and motor development of premature children in the cities of Bogotá and Tunja in comparison with the traditional kangaroo program
Methodology Experimental study with pretestposttest design with experimental and control group which determines the baseline With initial evaluation of the groups randomized assignment and post-intervention evaluation at 4 weeks and flow-up at 8 weeks The intervention will be developed in two scenarios in the outpatient kangaroo plan consultation and at home The experimental group will receive an intervention based on the promotion of maternal self-efficacy and the motor development of the premature baby The control group will have traditional kangaroo program care The sample calculation is 92 participants 46 in the experimental group and 46 in the control group The intervention evaluations and data analysis will be developed by blinded professionals An analysis of the data will be done by intention to treat
Type of results expected to be obtained It is expected to obtain an intervention that promotes maternal self-efficacy for the adequate stimulation of the motor development of the premature baby It is expected to enhance the confidence and empowerment of the maternal role the motor development of children in accordance with the corrected age and the incorporation of ICT for monitoring at home
Objective Determine the effect of an interdisciplinary intervention program on maternal self-efficacy and motor development of premature children in the cities of Bogotá and Tunja in comparison with the traditional kangaroo program
Methodology Experimental study with pretestposttest design with experimental and control group which determines the baseline With initial evaluation of the groups randomized assignment and post-intervention evaluation at 4 weeks and flow-up at 8 weeks The intervention will be developed in two scenarios in the outpatient kangaroo plan consultation and at home The experimental group will receive an intervention based on the promotion of maternal self-efficacy and the motor development of the premature baby The control group will have traditional kangaroo program care The sample calculation is 92 participants 46 in the experimental group and 46 in the control group The intervention evaluations and data analysis will be developed by blinded professionals An analysis of the data will be done by intention to treat
Type of results expected to be obtained It is expected to obtain an intervention that promotes maternal self-efficacy for the adequate stimulation of the motor development of the premature baby It is expected to enhance the confidence and empowerment of the maternal role the motor development of children in accordance with the corrected age and the incorporation of ICT for monitoring at home
Detailed Description:
None
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