N/A
N=42
Family Based Mindfulness Intervention
Parental Stress · Parent and Child Stress · Parental and Child Obesity · Child Obesity
Bottom Line
View on ClinicalTrials.gov: NCT01974102 ↗Enrolled (actual)
42
Serious AEs
0.0%
Results posted
Apr 2021
Primary outcome: Primary: Attendance — 5.7; 7.1 Sessions — p=<0.015
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Lifestyle counseling (Behavioral); Parenting Mindfully for Health (PMH) (Behavioral)
- Age
- Pediatric, Adult, Older Adult · 2+ yrs
- Sex
- All
- Sponsor
- Yale University
- Primary completion
- Oct 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Attendance |
5.7; 7.1 | <0.015 sig |
| SECONDARY Change in BMI Percentile |
12; 1.1 | <0.03 sig |
Summary
The goal of the proposed interdisciplinary study is to assess feasibility of recruiting a pilot sample of parents of toddlers and engaging them in a pilot study to test a version of mindfulness-based intervention for parenting stress reduction (PMH), an empirically-supported stress-reduction intervention, plus nutrition and physical activity counseling for parents of preschoolers (aged 2-5); to reduce parent (and child) stress levels; improve parenting; promote healthy eating and physical activity in parent and child; and prevent overweight and obesity in preschoolers with an obese parent.
Eligibility Criteria
Inclusion Criteria
- Between ages 18-70 years;
- Able to read and write (parent)
- Family with a child between 2-5 years old
- BMI of parent in obese category
- High parenting stress (mean score of >=3 on 3 questions from Parenting Stress Index)
Exclusion Criteria
- Any psychotic disorder or current psychiatric symptoms for child or parent requiring specific attention, including active symptoms of psychosis or suicidal/homicidal ideation
- Diagnosis of mental retardation, autism or other pervasive developmental disorder for child
- Inability to give informed consent
- Current serious medical disorder precluding participation in physical activity
Data sourced from ClinicalTrials.gov (NCT01974102). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.