- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03698110
Programa PUEDES Infancia (PUEDES)
October 4, 2018 updated by: Cayetana Ruiz Zaldibar, University of Navarra
Programa Padres y Madres Unidos Educando en Estilos de Vida Saludables
The purpose of this study was to evaluate whether an intervention directed at promoting parental self-efficacy and skills, based on a positive parenting framework, improves parental competences and healthy practices in families with children aged 2 to 5 years old.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study has designed implemented and evaluated an intervention to promote parental competence and healthy practices in families with children aged 2 to 5 years old, addressing parental self-efficacy an skills.
This research followed the first three stages of the Medical Research Council framework for complex interventions: the theoretical, modeling and exploratory trial phases.
A randomized control trial with parents of children better 2 to 5 years old was conducted.
The program consisted of two hour long four sessions.
Parents were grouped in small groups (7-8 participants) and guided by a facilitator whose role was to provide a participative and trusting atmosphere to share opinions and experience in healthy lifestyles and parenting.
Data collection was performed at three time points (pre-intervention, post-intervention and follow-up) to asses the preliminary efficacy, acceptability and feasibility of the program.
Study Type
Interventional
Enrollment (Actual)
23
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Navarra
-
Pamplona, Navarra, Spain, 31008
- Universidad de Navarra
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Be father or mother of at list one child between 2 to 5 years old
- Be over 18 years old
- Sign the informed consent
Exclusion Criteria:
- Fathers or mothers that could have special necessities that could prevent the course of the sessions
- Participants the could understand or speak spanish
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group
Participated in one introductory session, in the four sessions of PUEDES program during four weeks and in a closing session.
|
PUEDES program included eight hours in groups and activities to practice at home.
Other Names:
|
|
No Intervention: Control Group
Participated in one introductory session and in a closing session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline Parental Self-efficacy at post-intervention and three months. Tool to Measure Parental Self-efficacy (TOPSE) is a questionnaire developed to measure parental self-efficacy.
Time Frame: baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
Parenting self-efficacy (PSE) describes a parent's belief in their ability to perform the parenting role successfully.
Tool to Measure Parental Self-efficacy (TOPSE) is specifically useful for the evaluation of parenting programs.
TOPSE has 8 subscales about emotion and affection, play and enjoyment, empathy and understanding, control, discipline and boundaries, external pressures on parenting, acceptance of oneself and learning and knowledge.Regarding the validity and reliability of the scale varies between 0.80 and 0.89 per item, and of 0.94 as a whole (Kendall and Bloomfield, 2005).
|
baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
|
Change from baseline Parenting styles at post-intervention and three months. Parenting styles scale is a validated tool to measure the different types of parenting styles (democratic, authoritative, permissive or negligent).
Time Frame: baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
Parenting styles are the differences strategies that parents use in their child rearing.
Parenting style scale called Escala de Evaluación de Estilos Educativos (4E), measures the different types of parenting styles (democratic, authoritative, permissive or negligent).It evaluates, through 20 items on a Likert scale the posture of parents in the traditional dimensions of educational styles: affection and communication, demands and control.The reliability coefficient of Cronbach's alpha of the scale is 0.73 (Sánchez-Sandoval, León and Román, 2012).
|
baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
|
Change from baseline Parenting Practice in health promotion at post-intervention and three months. Meals in our household is a parent-report questionnaire that measures six domains related to the families' mealtimes.
Time Frame: baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
They are difference practices that parents practice in there daily life that could promote healthy habits in their families.Questionnaire Meals in our household will be used to assess structure of family meals, problematic child mealtime behaviours, use of food as reward, parental concern about child diet, spousal stress related to child's mealtime behaviour, influence of child's food preferences on what other family members eat.
The reliability coefficient of Cronbach's alpha is 0.77 (Anderson et al. 2012).
|
baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
|
Change from baseline Parenting Practice in health promotion at post-intervention and three months. Comprehensive Feeding Practice is a questionnaire focused on parents practice related to meals.
Time Frame: baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
Comprehensive Feeding Practice Questionnaire is reported by parents and assess the children involvement in meal planning and preparation and parental role model focused on if parents actively demonstrate healthy eating for the child.
|
baseline (before starting the program), post-intervention (5 weeks) and follow-up (3 months after the end of the program)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental satisfaction with the program. Questionnaire developed by researchers.
Time Frame: Post-intervention (5 weeks).
|
Parents from the intervention group will be asked about their parental satisfaction with the program.
Their opinion about its need, and whether they will be able to recommend it to friends or family, using a Likert scale of 0 to 10 developed by researchers, where 0 is nothing and 10 is completely, also were questions of this questionnaire.
|
Post-intervention (5 weeks).
|
|
Positive parenting program evaluation. The Evaluation system of positive parenting programs is a scale developed to assess positive parenting programs.
Time Frame: Post-intervention (5 weeks).
|
The Evaluation system of positive parenting programs was designed to evaluate the interventions in positive parenting in Spain (Manzano et al., 2012).
It is a tool that professional could use in the implementation, methodology and content of the program.
The system has 17 indicators that refer to different aspects of intervention programs such as general assessment, objectives, materials, evaluation or ethical aspects.
The results will be collected in a table that will show the scores of all the indicators, the total score of each thematic block and the final score obtained in the instrument.
In this way it will be observed what parts of the program have more power and which should be improved.
|
Post-intervention (5 weeks).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Musher-Eizenman D, Holub S. Comprehensive Feeding Practices Questionnaire: validation of a new measure of parental feeding practices. J Pediatr Psychol. 2007 Sep;32(8):960-72. doi: 10.1093/jpepsy/jsm037. Epub 2007 May 28.
- Anderson SE, Must A, Curtin C, Bandini LG. Meals in Our Household: reliability and initial validation of a questionnaire to assess child mealtime behaviors and family mealtime environments. J Acad Nutr Diet. 2012 Feb;112(2):276-84. doi: 10.1016/j.jada.2011.08.035.
- Kendall S, Bloomfield L. Developing and validating a tool to measure parenting self-efficacy. J Adv Nurs. 2005 Jul;51(2):174-81. doi: 10.1111/j.1365-2648.2005.03479.x.
- Sánchez-Sandoval Y, León E, Román M. Adaptación familiar de niños y niñas adoptados internacionalmente. Anales de psicología 28(2): 558-566, 2012
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 30, 2017
Primary Completion (Actual)
June 1, 2017
Study Completion (Actual)
November 17, 2017
Study Registration Dates
First Submitted
November 17, 2017
First Submitted That Met QC Criteria
October 4, 2018
First Posted (Actual)
October 5, 2018
Study Record Updates
Last Update Posted (Actual)
October 5, 2018
Last Update Submitted That Met QC Criteria
October 4, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 2017.025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Parenting
-
Johns Hopkins UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development...Recruiting
-
Tampere University HospitalTampere UniversityCompletedParenting Satisfaction | Parenting Self-efficacyFinland
-
Johns Hopkins UniversityThe Rita and Alex Hillman Foundation; Abell Foundation; Richman Foundation; Sherman... and other collaboratorsRecruitingParenting | Parenting InterventionUnited States
-
Aga Khan UniversityAga Khan Health Services; Global Affairs CanadaRecruiting
-
Georgetown UniversityRecruiting
-
University of MinnesotaCompletedParentingUnited States
-
University of South FloridaEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedParentingUnited States
-
King Abdullah International Medical Research CenterYale UniversityUnknownParentingSaudi Arabia
-
Boston Medical CenterHRSA/Maternal and Child Health BureauCompletedParentingUnited States
-
Fathers' Support Center, St. LouisWashington University School of MedicineUnknown
Clinical Trials on Intervention Group
-
Muğla Sıtkı Koçman UniversityNot yet recruiting
-
University of LiegeCentre Hospitalier Universitaire de Liege; Bial Foundation; FNRS (Télévie); Fondation...Active, not recruitingPain | Cancer | Fatigue | Cognitive Impairment | Sleep Disturbance | Distress, EmotionalBelgium
-
Beijing HospitalThe First Hospital of Jilin University; Jilin University; Chinese Academy of...Not yet recruitingAsthma | Allergic Disease
-
Hospital de Clinicas de Porto AlegreUnknown
-
University of California, San FranciscoNational Cancer Institute (NCI); Cancer Prevention Institute of CaliforniaCompletedHereditary Breast and Ovarian Cancer Syndrome
-
University of Sao PauloCompletedAnxiety | Self Esteem
-
Shenzhen Salubris Pharmaceuticals Co., Ltd.Salubris (Suzhou) Pharmaceutical Co., Ltd.RecruitingPostmenopausal Women With OsteoporosisChina
-
Haute Ecole de Santé VaudCompletedArthroplasty, Replacement, Knee | Arthroplasty, Replacement, HipSwitzerland
-
University of North Carolina, Chapel HillNational Heart, Lung, and Blood Institute (NHLBI)CompletedHeart Diseases | Cardiovascular Diseases
-
University of OxfordOxford Brookes UniversityRecruitingOverweight/Obesity, AdolescentUnited Kingdom