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Digital Universal Parenting Program for Positive Parenting Behaviors

U

University of Turku

Status

Enrolling

Conditions

Parenting

Treatments

Behavioral: Digitally Delivered Parent Training

Study type

Interventional

Funder types

Other

Identifiers

NCT06750510
BePresent

Details and patient eligibility

About

The goal of this study is to evaluate use and feasibility of digitally-delivered universal parenting program, which aims to promote positive parenting among guardians with 3 years-old children.

Full description

The study will use a single-arm study design.The participants will use the universal parenting program for 8-weeks.

The intervention is a digital parent training program which focuses on positive parenting and encouraging to develop parenting skills that strengthen the relationships and communication with their children. The topics includes for example reinforcing child´s positive behavior, reducing conflict situations and planning situations advanced, managing daily transitions, and being present to child. The program includes 5 themes with recommended length of 1 week each. Each theme includes theory material, videos, examples, video practices and exercises. The program is fully digital and provided in a dynamic, web-based format. SMS and email reminders will be sent regularly during the program.

Recruitment: All parents with a 3-year old child who is participating in annual health checkup in child health clinic are considered eligible to the study and are asked to participate if they fulfil inclusion criteria and do not meet the exclusion criteria.

Enrollment

1,500 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Guardians having a child aged 3 years participating to annual health checkup in child health clinic.
  • At least one of the guardians is able to understand the languages that intervention is provided in

Exclusion criteria

  • Inability to read Finnish, Swedish, or English, as these are the languages that the intervention is provided in.
  • No internet access

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,500 participants in 1 patient group

Intervention
Experimental group
Description:
Participants assigned to this condition will receive the 8-weeks intervention
Treatment:
Behavioral: Digitally Delivered Parent Training

Trial contacts and locations

2

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Central trial contact

Kaisa Mishina, PhD

Data sourced from clinicaltrials.gov

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