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Clinical Trials in Portugal / NCT07534111
Starting soon Not applicable

Preliminary Efficacy of the AdoptMindful2Care@Web: A Web-Based Mindful Parenting Post-Adoption Intervention for Adoptive Parents

NCT07534111 · tracked via the Priya Life Science Portugal tracker
Phase
Not applicable
Started
2026-04
Last updated
2026-04-21

Condition(s) studied

Parenting StressPositive Mental Health

Investigational drug(s) / intervention(s)

pAdoptMindful2Care@Web

pAdoptMindful2Care@Web: AdoptMindful2Care@Web is a universal, preventive, web-based mindful parenting intervention for adoptive parents, adapted from its face-to-face version (AdoptMindful2Care). Delivered through an online platform, it includes eight self-guided core modules (approximately 40 minutes each) and one follow-up module. The core modules are sequential and unlocked upon completion of the previous one, with no fixed schedule. The follow-up module becomes available one month after completion of the final core module. Each module combines multimedia resources, including psychologist-recorded videos, animated videos, audio-guided exercises, and interactive/animated texts, to enhance engagement and accessibility. The intervention integrates psychoeducation, mindfulness-based exercises, mindful parenting and self-compassion practices, and strategies informed by Cognitive Behavioral Therapy (CBT), aiming to prevent or reduce parenting stress and promote positive parenting practices.

Study summary

The development of post-adoption interventions aimed at promoting parental well-being and positive parenting is an urgent need. Mindful Parenting-based interventions appear to be particularly promising in this field, as they address parents' needs in coping with the emotional challenges of parenting and seem to foster greater compassionate, non-judgmental acceptance toward themselves and their children, as well as enhance the self-regulation of immediate emotional states in favor of long-term goals that support the parent-child relationship. However, the delivery of such interventions in face-to-face formats for adoptive parents (APs), particularly within the scope of universal prevention, faces considerable barriers (e.g., wide geographical dispersion of APs, limited mental health specialization among adoption service teams). eHealth tools represent an innovative pathway for intervention that may help overcome these barriers, given their multiple advantages, including: (1) improved access to healthcare regardless of time and location, (2) greater user autonomy in managing their own care, and (3) enhanced quality and innovation in service delivery, supported by the diversity, efficiency, and technological advancement of these systems. The primary goal of this study is to evaluate the effectiveness of AdoptMindful2Care@Web, a new 9-module, web-based post-adoption psychological intervention grounded in the principles of mindful parenting.

This pilot randomized controlled trial, with a two-arm design, precedes the full RCT planned as AdoptMindful2Care@Web. It is open to mothers and fathers who have at least one adoptive child under 18 years of age, whose adoption was legally decreed by the court less than 24 months prior to enrollment, who are not involved in any other ongoing adoption process, who are able to read and write in Portuguese, and who have regular access to the internet and electronic devices. A minimum of 90 families will be recruited with the support of all Portuguese governmental adoption agencies. After expressing interest in participating through an expression-of-interest form available on the project website, a member of the research team will contact them by telephone to conduct an initial screening (brief interview), with the following aims: (1) to clarify any questions regarding the study and (2) to assess their eligibility for participation (i.e., to confirm whether they meet the inclusion criteria and do not fall under any exclusion criteria). At the end of the telephone screening, they will be informed of the decision of eligibility. If deemed eligible and willing to participate, a specific date and time will be scheduled for completion of the online study assessment protocol corresponding to the first assessment point (T0). To support adherence to this appointment, a reminder will be sent on the scheduled day (via text message or email, as applicable).

Eligible participants will be randomly assigned to either the intervention group (AdoptMindful2Care@Web) or a waitlist control group (participants will receive the intervention after the study concludes). The intervention includes eight core modules plus a follow-up module, all carried out via an online platform, each lasting approximately 40 minutes. Participants in both groups will complete assessments at four time points: baseline, post-intervention, 1- and 2-month follow-up. These assessments will include both self-report (e.g., parenting stress) and hetero-report measures (e.g., children's emotional and developmental difficulties).

Eligibility

Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
No
Inclusion Criteria: * Have at least one adoptive child aged under 18 years * Have an adoption decreed by the court less than 24 months ago * Have no other adoption process in progress * Have reading and writing abilities in the Portuguese language * Have regular access to the internet and electronic devices Exclusion Criteria: * Presence of a severe mental disorder (e.g., schizophrenia, substance abuse, bipolar disorder). * Have previously participated in the face-to-face, group-based version of the programme (pAdoptMindful2Care)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Psychology and Education Sciences, University of Coimbra Coimbra Portugal

More University of Coimbra trials in Portugal

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07534111 on ClinicalTrials.gov ↗ ← All trials in Portugal