Evaluation of the Family Intervention Program (PIF)

NCT07106775 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-08-14

No results posted yet for this study

Summary

The goal of this study is to evaluate the effectiveness of home positive parenting programs targeted to families at psychosocial risk carried out in Cantabria (Spain).

The investigators will collect information before the intervention, and every six months until the family achieves the proposed objectives (with a maximum intervention period of two years). Besides, the investigators will compare these results with information from other families that are not taking part in the program. Depending on the case, the practitioners in charge of the intervention, the main caregivers of the participating families and/or the adolescents will provide the information for the study.

The investigators expect that families participating in the programs will improve their parenting competencies, their family dynamics, and the life quality of their children.

Conditions

  • Parenting
  • Children/Adolescent Adjustment
  • Family Functioning

Interventions

BEHAVIORAL

Family Intervention Program (PIF)

Home psychoeducational intervention in an individual format driven by a practitioner where caregivers learn parenting competences and children learn autonomy and emotional regulation skills

Sponsors & Collaborators

  • Gobierno de Cantabria

    collaborator UNKNOWN
  • Loyola University

    collaborator OTHER
  • University of Jaen

    collaborator UNKNOWN
  • University of Seville

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-15
Primary Completion
2026-05-31
Completion
2026-05-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07106775 on ClinicalTrials.gov