Behavioral Parenting Skills As A Novel Target for Improving Pediatric Medication Adherence

Sponsor
Roswell Park Cancer Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT05587582
Collaborator
National Cancer Institute (NCI) (NIH)
79
1
51
1.6

Study Details

Study Description

Brief Summary

This study observes behavioral parenting skills to see whether it could be a novel target for improving pediatric medication adherence. This study may help researchers better understand the challenges parents face when giving their young child with an illness medicine at home and learn about various factors related to medication compliance in young children

Condition or Disease Intervention/Treatment Phase
  • Other: Survey Administration

Detailed Description

PRIMARY OBJECTIVES:
  1. Use direct observation of medication administration in the home to understand common episode-level barriers and identify the most impactful behavioral parenting skills for intervention.

  2. Use daily diary methods to identify contextual barriers to adherence and identify intervention components to help parents anticipate barriers and plan strategies to promote successful adherence.

OUTLINE:

Participants complete a survey over 15-20 minutes at baseline. Family behaviors before, during and after the administration of medication to the child are video-recorded over 40-45 minutes. Participants receive MEMS electronic pill bottle to use for 2 weeks and complete daily survey over 5 minutes for 14 days.

Study Design

Study Type:
Observational
Anticipated Enrollment :
79 participants
Observational Model:
Family-Based
Time Perspective:
Cross-Sectional
Official Title:
Behavioral Parenting Skills as a Novel Target for Improving Pediatric Medication Adherence: Studies 1 and 2
Actual Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Nov 30, 2026
Anticipated Study Completion Date :
Nov 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Observational (Family Behaviors)

PRIMARY OBJECTIVES: I. Use direct observation of medication administration in the home to understand common episode-level barriers and identify the most impactful behavioral parenting skills for intervention. II. Use daily diary methods to identify contextual barriers to adherence and identify intervention components to help parents anticipate barriers and plan strategies to promote successful adherence. OUTLINE: Participants complete a survey over 15-20 minutes at baseline. Family behaviors before, during and after the administration of medication to the child are video-recorded over 40-45 minutes. Participants receive MEMS electronic pill bottle to use for 2 weeks and complete daily survey over 5 minutes for 14 days.

Other: Survey Administration
Complete a survey

Outcome Measures

Primary Outcome Measures

  1. Dyadic Parent-Child Interaction Coding System (DCIPS) - medication ingestion [Up to 5 months]

    Association between ingestion of medication and the absence or presence of each of the Observations of parents and children as they interact with each other during medication administration. Interactions will be coded by trained observers.

  2. Length of time it takes to administer medication [Up to 5 months]

    The association between time to ingestion and the DCIPS coded skills will be analyzed

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
INCLUSION:
  • Parent of a child diagnosed within the past month with acute lymphoblastic leukemia (ALL)

  • Pediatric patient's age 3 - 9.

  • If present during the home visit, any other child, ages 0-18
  • Child on therapy that includes oral mercaptopurine (6-MP) administration

  • Parent age 18 - NA (No Limit)

  • Parent should have verbal English fluency

  • Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure

  • The following special populations may be included in this study:

  • Pregnant women: due to the design of this behavioral research, pregnant and fetuses should incur no elevated risk from participation.

Children under age 18 will participate in one aspect of the study, the video recording of medication administration.

  • Other children (not the pediatric patient) under age 18 that are present during the time of the home visit
Exclusion:
  • Pediatric patient is on therapy that does not include oral 6-MP administration

  • Cognitively impaired adults/adults with impaired decision-making capacity

  • Pediatric patients who are not yet adults (infants under the age of 3, children over 9 years, teenagers)

  • Prisoners

Contacts and Locations

Locations

Site City State Country Postal Code
1 Roswell Park Cancer Institute Buffalo New York United States 14263

Sponsors and Collaborators

  • Roswell Park Cancer Institute
  • National Cancer Institute (NCI)

Investigators

  • Principal Investigator: Elizabeth Bouchard, PhD, Roswell Park Comprehensive Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Roswell Park Cancer Institute
ClinicalTrials.gov Identifier:
NCT05587582
Other Study ID Numbers:
  • I 1832021
  • R01CA258337
First Posted:
Oct 20, 2022
Last Update Posted:
Nov 10, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 10, 2022