Testing Design Thinking Methodology to Engage Hispanic and Latino Families of Autistic Children in Research.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorThomas Jefferson University

About this trial

The goal of this study is to compare the level of engagement in the Hispanic and Latino parents of autistic children and culturally adapt the protocol of Ayres Sensory Integration to improve participation and health outcomes.

The main questions it aims to answer are:

Does the Design Thinking process result in higher stakeholder engagement and satisfaction in the research process in comparison to Focus Groups? Secondary question: Do cultural adaption using DT data yield higher scores of acceptability and implementation feasibility in comparison to FG methods?

Participants will:

* Be randomized into two groups of engagement (focus groups and design thinking) * Be blinded (clinicians, selected caregivers, autistic persons, and cultural experts) and will rate the acceptability, feasibility, and cultural appropriateness of the protocol based on DT data higher than the protocol based on FG data.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

confirmed diagnosis of autism spectrum disorder

Hispanic/Latino

received therapeutic services as a child; and

willing and able (with i.e., language and cognitive skills) to participate in the design thinking or focus group session designed to learn about the facilitator and barriers to receipt of therapeutic services.

Disqualifiers

Do not meet age for autistic individual or diagnostic criteria

Trial design

Design model

Parallel

Treatments tested in this trial

  • Design Thinking

    Other intervention

    Participants attend the DT session through all the stages that include emphasize, define, ideate, prototype and test.

  • Focus Groups

    Other intervention

    Participants attend the FG that includes the introduction. discussion, and reflection.

Treatment groups

186 Participants
are divided into 2 treatment groups
Group A: Design Thinking GroupOther 1 intervention
Group B: Focus GroupOther 1 intervention

Trial outcomes

Primary outcomes

1

Stakeholder-Centric Engagement Evaluation

The instrument evaluates stakeholder engagement via the PCORI engagement principles. DT and FG participants use this instrument to rate engagement in throughout the research process using a Likert scale with 1= never and 5 = always.

Time frame
up to 14 weeks

Secondary outcomes

1

Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM) and the Feasibility of Intervention Measure (FIM) (Weiner et al., 2017)

These are outcome measures that evaluate implementation success via the extent to which stakeholders believe the intervention is acceptable, appropriate, and feasible. Each measure uses a Likert response scale where 1 = completely disagree and 5 = completely agree.

Time frame
up to 14 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Thomas Jefferson University

Lead sponsor

Patient-Centered Outcomes Research Institute

Collaborator

This trial is not recruiting at the moment. You can still explore other options: