Choice and Autonomy in Learning Mindfulness for Pediatric Residents

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorNorthwestern University

About this trial

This study is a pilot clinical trial designed to evaluate a flexible, online mindfulness program for pediatric residents. Medical training can be stressful, and although mindfulness programs are often offered to support well-being, many are either in-person or follow a fixed format that may not fit individual schedules or preferences. This study will test a digital mindfulness program called Wakeful, which allows participants to complete the course at their own pace. Participants will be randomly assigned to one of two groups: one group will be able to choose the length of their mindfulness program (3, 5, or 7 weeks), while the other group will be assigned a program length without a choice. The goal is to understand whether giving participants a choice improves how often they use the program, how satisfied they are with it, and whether they complete it. The main outcomes of this study focus on how participants interact with the program, including how many sessions they complete, how often they practice mindfulness on their own, and how useful and relevant they find the program. The study will also look at overall satisfaction and how many participants drop out before finishing. In addition, the study will explore whether participants report changes in mindfulness and compassion for others, although it is not designed to determine clinical improvements in mental health. By understanding how pediatric residents engage with different program formats, this study aims to inform the design of more flexible and user-centered digital wellness programs that better fit into demanding medical training environments.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Current categorical pediatrics residents at Northwestern University.

Preliminary pediatrics residents who intend to continue in pediatrics.

Willing and able to provide informed consent.

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Wakeful Digital Mindfulness Program

    Behavioral

    Wakeful digital mindfulness program: an asynchronous, web-based course with guided meditations, didactic content, and optional reflective exercises.

Treatment groups

42 Participants
are divided into 2 treatment groups
Group A: ChoiceExperimental treatment 1 intervention
Group B: No ChoiceExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Engagement and completion of Wakeful program modules

The primary outcome measures participant engagement with the Wakeful digital mindfulness program, including (1) the number of program modules completed, (2) frequency and duration of platform use, (3) frequency of independent meditation practice, (4) perceived usability and relevance, and (5) overall satisfaction and dropout rates. All measures are collected via de-identified platform usage data and post-intervention surveys to assess acceptability and adherence.

Time frame
Baseline and immediately post-intervention (3, 5, or 7 weeks depending on program length)

Secondary outcomes

1

Changes in mindfulness, self-compassion, and compassion for others

Exploratory outcomes assess trends in psychological constructs following the Wakeful digital mindfulness program. Measures include mindfulness using the PROMIS Global Mindfulness Measure, self-compassion using the Neff Self-Compassion Scale, and compassion for others using the Neff Compassion Scale. These surveys are completed at baseline and post-intervention. The study is not powered for statistical comparisons; analyses are descriptive to guide future intervention design.

Time frame
Baseline and immediately post-intervention (3, 5, or 7 weeks depending on program length)

Other outcomes

Sponsors and contacts

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