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
Not provided
This is a concept elicitation study to identify important aspects of pain assessment, treatment, and response to treatment in children under than 3 years of age from a caregiver's perspective.
The purpose of this study is to identify important endpoints and outcomes for use in pediatric trials for acute pain therapeutics in infants and young children from a caregiver's perception. Study team members will conduct phone-based qualitative interviews, using a semi-structured interview guide, with 42 primary caregivers of pediatric patients under 3 years of age who are experiencing or have experienced acute pain. Once participants give verbal consent, they will fill out a demographics form. Interviews will last about one hour and will address the participant's experience recognizing and managing their child's acute pain. The investigators will use these concept elicitation interviews to identify important aspects of acute pain assessment, treatment, and response to treatment in children who are under 3 years old. Interviews will be audio recorded and transcribed with participant permission. Transcripts or interviewer notes will be reviewed by two analysts and will be double coded until inter-rater reliability is reached by agreement of at least 80%. The study team will conduct a thematic analysis of the coded transcripts. This is a minimal risk study. All information will be kept confidential and information will be stored on a secure network which is only accessible to the study team.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Caregivers | Caregivers who care for a child that is both under 3 years of age and has experienced acute pain. This cohort will participate in a qualitative interview about pain assessment, treatment, and response to treatment in their child. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Qualitative Interview | Other | There is no intervention as part of this study. Caregivers will participate in a qualitative interview over the phone or by video. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Caregiver perspective on how to identify or recognize pain in children 0 to <3 years old. | A 1-hour qualitative interview will be conducted and transcript or interviewer notes will be coded to assess how caregivers identify and recognize acute pain in infants and young children. | 1 hour |
| Caregiver perspective on how and when to intervene for acute pain in children 0 to <3 years old. | A 1-hour qualitative interview will be conducted and transcript or interviewer notes will be coded to assess caregiver's perspective on how and when to treat acute pain in infants and young children. | 1 hour |
| Caregiver perspective on how to evaluate response to treatment for acute pain in children 0 to <3 years old. | A 1-hour qualitative interview will be conducted and transcript or interviewer notes will be coded to assess how caregivers evaluate response to treatment for acute pain in infants and young children. | 1 hour |
| Caregiver perspective on important side effects of acute pain therapeutics in children 0 to <3 years old. | A 1-hour qualitative interview will be conducted and transcript or interviewer notes will be coded to assess caregiver's perspective on important side effects of acute pain in infants and young children. | 1 hour |
Not provided
Not provided
Inclusion Criteria:
Cares for a child who is both:
Is over the age of 18 years old.
Can speak and understand English.
Is capable of and willing to provide informed consent for interview participation and to collect medical data from the child's medical record.
Exclusion Criteria:
Not provided
Not provided
Not provided
The study population will be caregivers of children 0 to <3 years old who have experienced acute pain. Eligible caregivers will be identified by Pediatric Trials Network sites across the United States. Eligible participants will be identified through recruitment for a pre-existing Pediatric Trials Network study called Pharmacokinetics and Safety of Anesthetics and Analgesics in Children and Adolescents.
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
| ID | Term |
|---|---|
| D059787 | Acute Pain |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
Not provided
Not provided
Not provided
Not provided
Not provided