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Clinical Trials/NCT06285552
NCT06285552
Recruiting
Not Applicable

Evaluation of the Comprehensive Family Support Program (PAIF)

University of Seville1 site in 1 country300 target enrollmentFebruary 20, 2024
ConditionsParenting

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parenting
Sponsor
University of Seville
Enrollment
300
Locations
1
Primary Endpoint
Parenting practices (Overreactivity and Laxness)
Status
Recruiting
Last Updated
9 months ago

Overview

Brief Summary

The goal of this study is to evaluate the effectiveness of positive parenting programs targeted to parents of toddlers, children and adolescents carried out in Cantabria (Spain).

We will collect information from the participants before the intervention, in the last session of the program and some months after, to verify if there have been some changes in the family dynamics of these parents, and if these changes continue after some time. Besides, we will compare these results with information from other families that are not taking part in the program. The main caregivers of the participating families and the practitioners in charge of the intervention will provide the information for the study.

We expect that families participating in the programs will improve their parenting competencies and their family dynamics, and that these change will stay after the program.

Detailed Description

A quasi-experimental design will be followed, with three evaluation moments (pretest, posttest and follow-up) and with a non-randomized comparison group. The positive parenting programs will be advertised by social media, schools and high schools. The participants will be parental figures interested in joining these programs. The participants will answer a series of questionnaires by an app, where they will give information related to sociodemographic data and parenting competencies. The app will not allow the participants to leave any question with no answer or with an incorrect answer. To analyze the data, we will use the softwares Mplus and Statistical Package for the Social Sciences (SPSS).

Registry
clinicaltrials.gov
Start Date
February 20, 2024
End Date
October 1, 2025
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Victoria Hidalgo García

Principal Investigator

University of Seville

Eligibility Criteria

Inclusion Criteria

  • Being caregiver of at least one child under 18 years of age
  • The child to be in the developmental stage appropriate for the corresponding arm
  • If participating in a targeted program, meet the requirements: (1) be a father; (2) presenting bad health habits in the family according the evaluation of the pediatrician
  • Motivated to improve parenting competences

Exclusion Criteria

  • Not having sufficient command of the Spanish language to be able to communicate
  • Experience family crisis that prevent for participating in a group intervention
  • Experience mental health issue that prevent for participating in a group intervention

Outcomes

Primary Outcomes

Parenting practices (Overreactivity and Laxness)

Time Frame: Pretest, immediately posttest and 6 month follow-up

Parenting Scale - Short version (PS), rated on a 7-point Likert-type scale ranging from 1 to 7. Higher scores mean a worse outcome.

Perception of the parental role

Time Frame: Pretest, immediately posttest and 6 month follow-up

Me as a Parent Scale (MaaP), rated on a 5-point Likert-type scale ranging from 1 to 5. Higher scores mean a better outcome.

Parenting practices (Authoritative parenting style: Warmth and Support, Reasoning/Induction, Democratic Participation)

Time Frame: Pretest, immediately posttest and 6 month follow-up

Parenting Styles and Dimensions Questionnaire - Short version (PSDQ-Short version), rated on a 5-point Likert-type scale ranging from 1 to 5. Higher scores mean a better outcome.

Secondary Outcomes

  • Social support(Pretest, immediately posttest and 6 month follow-up)
  • Satisfaction with the intervention(Immediately Posttest)
  • Satisfaction with Family Life(Pretest, posttest and follow-up)
  • Children adjustment(Pretest, immediately posttest and 6 month follow-up)

Study Sites (1)

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