ClinicalTrials.Veeva

Menu

Online Parenting Support With VIPP-SD in Chile (VIPP-SD Chile)

U

Universidad San Sebastián

Status

Not yet enrolling

Conditions

Burnout
Parents

Treatments

Behavioral: Video Intervention to Promote Positive Parenting and sensitive discipline (VIPP-SD)

Study type

Interventional

Funder types

Other

Identifiers

NCT07365189
1252183 (Other Grant/Funding Number)
CEC N°69-25

Details and patient eligibility

About

The goal of this randomized controlled trial is to test whether the online Video-feedback Intervention to Promote Positive Parenting and Sensitive Discipline (VIPP-SD) can reduce parental burnout and improve parenting practices, in mothers of young children in Chile.

The main questions it aims to answer are:

  • Does the online VIPP-SD increase maternal sensitivity and the use of consistent but gentle limit setting?
  • Does it reduce parental burnout?
  • Does it improve parental stress and child attachment security and reduce child conduct problems? Researchers will compare families who receive the online VIPP-SD to families in a waitlist control group with dummy treatment to see if VIPP-SD has benefits for parents and children.

Participants will be mothers of children aged 11-16 months at the start of the study who report elevated levels of parental burnout. Mothers in the intervention group will:

  • Take part in 12 weekly online sessions with a trained intervener
  • Receive video-feedback on their own interactions with their child
  • Learn strategies to respond sensitively to their child's needs and to use positive discipline The study will also measure potential moderators such as maternal mental health, child temperament, and family sociodemographic factors.

Enrollment

140 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Mothers >18 years
  • Child age between 11 - 16 months old at first contact
  • Mothers scoring in the top 30% of our sample on the Parental Burnout Scale (BPPS)
  • Written informed consent of mothers as participants and guardians
  • Internet connection at mother's home.

Exclusion criteria

  • Child or parent with severe sensory impairment, learning disability, or language limitation
  • Sibling already participating in the trial
  • Family participating in active family court proceedings
  • Parent participating in another closely related research trial and/or receiving an individual video-feedback intervention.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

140 participants in 2 patient groups

Control Group
No Intervention group
Description:
Families in the control group will be contacted online individually by a psychologist (different from interveners) six times to discuss parenting strategies and child development, serving as an active control group. Later, they will receive the online VIPP-SD intervention in the experimental group by the same group of interveners.
Experimental Group
Experimental group
Description:
The intervention is delivered through a videoconference platform that allows 1) to record the parent-child tasks and 2) to simultaneously share the previously recorded parent- child interaction and provide feedback. The intervener provides directions in the recording sessions that ensure clearly capturing parent and child facial expressions during the task. Moreover, considering the delivery format, it is essential that both parents and interveners have access to good-quality internet and an electronic device (mobile phone, computer, tablet) with camera. To prevent fatigue arising from the delivery format, it was decided to shorten the sessions, with 30-minute sessions for recording the parent-child task and 40-60-minute sessions for video reviewing and feedback. Thus, Online-VIPP has 12 sessions with alternating recording sessions and video feedback sessions.
Treatment:
Behavioral: Video Intervention to Promote Positive Parenting and sensitive discipline (VIPP-SD)

Trial contacts and locations

0

Loading...

Central trial contact

RODRIGO A. CARCAMO LEIVA, Ph.D.; Jessica Vidal, Ph.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems