Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Food and Drug Administration (FDA) | FED |
Not provided
Not provided
Not provided
Not provided
This is a concept elicitation study to identify important aspects of acute pain assessment, treatment, and response to treatment in infants and young children, age 0 to 3 years old, from a clinician's perspective.
The purpose of this study is to identify important endpoints and outcomes for use in pediatric trials of acute pain therapeutics in children who are 0 to <3 years of age from a clinician's perspective. To identify these endpoints and outcomes the investigators will conduct remote qualitative concept elicitation interviews with 27 clinicians who treat pediatric patients. These interviews will include verbal consent to participate, a demographics questionnaire, and a semi-structured interview which will last approximately one hour. Interview questions will address the participant's professional experience recognizing and managing pain in children between 0 and 3 years of age. Interviews will be audio recorded and transcribed with the participant's permission. Transcripts and notes will be coded and analyzed. This is a minimal risk study; the investigators are only using standard interview procedures and are not collecting any protected health information from participants. While the investigators do not believe that any information collected would jeopardize the personal or professional standing of participants, all information will be kept strictly confidential per Good Clinical Practice guidelines.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Clinicians | Clinicians who care for pediatric patients >50% of their time, who treat pediatric patients who are in acute pain and between 0 and 3 years of age. May include physicians, clinical pharmacists, nurse practitioners, physician assistants, and/or nurses. This cohort will complete a qualitative interview about pain and distress in infants and young children. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Qualitative Interview | Other | There is no intervention as part of this study. Clinicians will participate in a qualitative interview. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Clinician perspectives on how to identify or recognize pain in children 0 to <3 years of age | A 1-hour qualitative interview will be conducted and transcript or interviewer notes coded to assess how clinicians identify and recognize acute pain in infants and young children | 1 hour |
| Clinician perspectives on how and when to treat acute pain in children 0 to <3 years of age | A 1-hour qualitative interview will be conducted and transcript or interviewer notes coded to assess how clinicians treat acute pain in infants and young children | 1 hour |
| Clinician perspectives on how to evaluate response to treatment for acute pain in children 0 to <3 years of age | A 1-hour qualitative interview will be conducted and transcript or interviewer notes coded to assess how clinicians evaluate response to treatment for acute pain in infants and young children | 1 hour |
| Clinician perspectives on important side effects of acute pain therapeutics in children 0 to <3 years of age | A 1-hour qualitative interview will be conducted and transcript or interviewer notes coded to assess important side effects of acute pain therapeutics in infants and young children | 1 hour |
Not provided
Not provided
Inclusion Criteria:
Is a practicing clinician in a clinical care environment
Cares for pediatric patients >50% of their time
Treats or works with pediatric patients who are between 0 and <3 years of age AND being treated for acute pain
Holds one of the following titles/positions
Is over the age of 18 years
Can speak and understand English
Is capable of giving informed verbal consent
Exclusion Criteria:
1. Lack of access to a telephone for interview
Not provided
Not provided
Not provided
The study population will be practicing clinicians who care for pediatric patients > 50% of their time, and who treat pediatric patients who are in acute pain and between 0 and 3 years of age
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Bryce Reeve, PhD | Duke University | Principal Investigator |
| Kanecia Zimmerman, MD, MPH | Duke University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Duke University | Durham | North Carolina | 27701 | United States |
Individual participant data will not be shared outside of the study team.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided