Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
ID04857775

Attachment and Child Health (ATTACH2) Program Adaptation and Pilot Testing Using Web and Mobile Interfaces

Led by University of Calgary · Updated on 2024-05-10

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

The trial investigates the adaptation and pilot testing of the ATTACH2 parenting program, originally designed for in-person delivery, to an online web and mobile format. The program aims to improve children's mental, emotional, and behavioral health by strengthening the parent-child relationship, particularly for families affected by stressors like depression, addiction, domestic violence, and poverty. This transition responds to challenges posed by the COVID-19 pandemic limiting in-person services and seeks to provide safe, user-friendly virtual mental health support to vulnerable families. The ATTACH2 program consists of 10 to 12 weekly sessions, each about 45 minutes, delivered by trained facilitators such as nurses or social workers. The study involves co-designing virtual interfaces with parents and service providers through four phases: user engagement and design exploration, prototyping, software development, and pilot beta testing. The goal is to create a reliable minimum viable product for virtual delivery that incorporates user feedback and meets the needs of families and facilitators. Participants will be involved in pilot testing the virtual program, with assessments conducted before and after the intervention to measure changes in children's mental, emotional, and behavioral health using age-appropriate tools. Parent-child interaction quality will be assessed using the Parent Child Interaction Teaching Scale. Data will be collected through surveys and focus groups, and refinements will be made based on participant feedback. The study also includes dried blood sample collection for participating families in specific locations, and the total intervention period spans about 10 to 12 weeks.

CONDITIONS

Brief Title

Adaptation and Pilot Testing of Web and Mobile Interface for the ATTACH™ Intervention

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Parent of a child between birth and 32 months of age
  • Agree to participate in 10 to 12 weekly parent training sessions lasting about one hour each
  • Agree to bring a co-parent to 2 to 3 of the sessions when possible
  • Agree to provide dried blood samples from self and child (if participating in Calgary agencies)
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or virtual)

Treatment

Duration - 10 to 12 weeks

Participants engage in weekly parent training sessions designed to improve Reflective Function (RF) and parent-child interactions using the ATTACH™ program delivered via web and mobile interfaces.

10 to 12 weekly sessions lasting about one hour each, including 2 to 3 sessions with a co-parent

Trial Site Locations

Total: 1 location

1

University of Calgary

Calgary, Alberta, Canada, T2N 1N4

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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