Using Parent Engagement to Improve the Wellbeing of Black Premature Infants With Chronic Lung Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohns Hopkins University

About this trial

The goal of this pilot study is to test the feasibility and acceptability of a collaborative goal setting intervention to improve parent engagement of Black preterm infants with chronic lung disease in primary care. Preliminary impact on child and parent outcomes will also be explored.

The main questions it aims to answer are: 1) Will parents complete a pre-visit questionnaire that asks about goals for the child? 2) Does use of the pre-visit questionnaire help parents to achieve self-identified goals?

Participants will fill out a pre-visit questionnaire prior to the child's well visit. The participants will then complete two surveys after the visit (1 week and 2 months after).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Parent/legal guardian of child born prior to 37 weeks gestational age

Parent/legal guardian of child with diagnosis of chronic lung disease or bronchopulmonary dysplasia, as defined by the child's clinical team at the time of hospital discharge

Parent/legal guardian of child who identifies that child's race as Black

English speaking

Disqualifiers

Parent/legal guardian of child enrolled in palliative care or hospice services at time of hospital discharge

Parent/legal guardian of child older than 12 months chronological age

Trial design

Design model

Single group

Treatments tested in this trial

  • P-CGS (Pediatric Collaborative Goal Setting)

    Behavioral

    Electronic questionnaire sent to participants ahead of a pediatric primary care well child visit, assessing goals for themselves and the child's health with prompt to share with providers during visit

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Pediatric Collaborative Goal Setting ParticipantExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility as measured by number of interventions completed

Number of participants who complete the pediatric collaborative goal setting intervention out of the number of consented participants who are sent a link prior to the child's well visit

Time frame
Day 0
2

Feasibility as measured by the time it takes participant to complete intervention

Amount of time (minutes) that participant has the pediatric collaborative goal setting intervention open

Time frame
Day 0
3

Feasibility as measured by the number of goals submitted by each participant

Number of goals submitted by each participant through the pediatric collaborative goal setting intervention

Time frame
Day 0
4

Acceptability of the intervention as assessed by the Acceptability of Intervention Measure (AIM) scale

Measured by the Acceptability of Intervention Measure (AIM) scale - a 4 item survey with 5 point Likert scales from Completely Disagree to Completely Agree. Score ranges from 4 to 20, where higher scores indicate greater acceptability.

Time frame
Day 7 post-intervention

Secondary outcomes

1

Goal attainment as assessed by number of goals submitted

Number of goals submitted as part of pediatric collaborative goal setting that were accomplished by participant since intervention

Time frame
Day 60 post-intervention
2

Participation activation as measured by Parent Patient Activation Measure 10

Measured by the Parent Patient Activation Measure scale - a 7 item survey with 4 point Likert scales (total score range 7-28) from Disagree Strongly to Agree Strongly with higher scores indicating a better outcome.

Time frame
Day 60 post-intervention
3

Participant's child's respiratory symptoms as measured by self-report

Frequency of rescue inhaler use and symptoms of wheezing, rated on 5 point Likert scale (total score range 1-5) from Never to Every day with higher scores indicating more use and worse outcome. This is a survey instrument constructed by the study team.

Time frame
Day 60 post-intervention
4

Participant's child's use of the emergency department for breathing symptoms as measured by self-report

Frequency of emergency department visits, rated on 5 point Likert scale (total score range 1-5) from Never to Every day with higher scores indicating more use and worse outcome. This is a survey instrument constructed by the study team.

Time frame
Day 60 post-intervention

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

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