Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06617299
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-09-24
Brief Title:
Cognitive-behavioral Intervention to Increase the Practice of Responsive Feeding and Maintain Healthy Weight in Infants
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Cognitive-Behavioral Intervention Targeting Mothers to Increase Practice of Responsive Feeding and Maintain Healthy Weight in Infants Minors
Status:
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:
None
Brief Summary:
Introduction Childhood overweight and obesity in Mexico is a serious public health problem Perceptive eating is a factor in the prevention of obesity and occurs when the caregiver recognizes the signs of hunger and satiety responds in a timely manner to these needs However its implementation is often a challenge for parents Studies show that there is low knowledge and self-efficacy as well as erroneous beliefs about food Teaching perceptive eating can lead to the development of healthy eating habits generate warm environments in which the interaction between parents and children is strengthened and promote self-regulation of hunger and satiety sensations and prevent overweight and obesity Interventions on Responsive Feeding for the prevention of healthy weight in infants under six months of age are null in Mexico Objective To evaluate the effect of the intervention 34Identify and Respond34 aimed at Mexican mothers to increase the practice of Responsive Feeding and maintain a healthy weight in children under 6 months of age Methodology The present study will be a pilot clinical trial type intervention study because the preliminary effect will be evaluated where the Experimental Group will receive the intervention aimed at increasing the practice of Responsive Feeding there will be randomization of repeated measurements by virtue of which measurements will be made at three times before the intervention baseline and follow-up post-test 3 and 6 months later The sample consisted of 72 mothers with children younger than 6 months for each group N144
Detailed Description:
None
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