Skip to content

Decision Aid for Parents of Infants With UPJO

Pilot-testing of a Decision Aid for Parents of Infants With Ureteropelvic Junction Obstruction (UPJO)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05900375
Enrollment
100
Registered
2023-06-12
Start date
2023-01-21
Completion date
2025-12-31
Last updated
2024-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ureteropelvic Junction Obstruction, Ureteropelvic Junction; Obstruction, Congenital

Keywords

shared decision making, pragmatic trial, congenital kidney anomaly

Brief summary

Ureteropelvic junction obstruction (UPJO) is the most common etiology of high-grade hydronephrosis, affecting approximately 4,000-10,000 infants annually in the U.S. The goal of surgical treatment of UPJO is to minimize the risk of kidney damage associated with obstruction, which may occur in 30-60% of infants with high-grade hydronephrosis.1-However, the benefit of early surgery compared to observation and potential later surgery to preserve kidney function has not been well-defined. Consequently, surgeons differ on whether to initially treat with surgery or observation, with surgical rates in the first year of life varying from 15-50% across surgical practices. These variations are important to understand, as the decision for early surgery is not without risk. Prior studies suggest that infants treated surgically are at higher risk for readmission and reoperation. Early surgery also raises concerns about neurodevelopmental effects of anesthetic exposure. To address this gap, the purpose of this pilot test is to develop a patient decision aid (PtDA) tool and pilot test its effect on parental understanding and engagement in the decision-making process at Children's Hospital Colorado. The proposed pilot is a necessary first step in preparation for a future multicenter hybrid effectiveness-implementation trial. This work will also be used to support future studies evaluating the impact of a PtDA on surgical variations and treatment outcomes in patients with UPJO and other complex congenital urologic anomalies.

Interventions

BEHAVIORALParent Decision Aid

A paper parent decision aid in color will be provided to all patients at the time of their appointment and will aid in discussion with health care professionals.

Sponsors

Children's Hospital Colorado
CollaboratorOTHER
University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

(all of following are needed): * parents (age 18-89 years) of children age 30 days - 2 years * child is presenting for consultation for SFU grade 3-4 Hydronephrosis at Children's Hospital Colorado * parents/child presenting at Urology appointment where a MAG 3 is performed or has recently been performed.

Exclusion criteria

* does not meet age parameters * does not have a child with a UPJO

Design outcomes

Primary

MeasureTime frameDescription
Differences in the SDM-Q9 scores between armsthrough study completion, an average of 1 yearThe primary outcome will be differences in scores between the 9-item Shared Decision Making Questionnaire (SDM-Q9) survey scores between intervention and control arms. The SDM-Q9 is a validated survey instrument measuring patient understanding and engagement in the decision making process. The scale for each question is 1-5 and higher scores mean better parent involvment and understanding.

Secondary

MeasureTime frameDescription
Assess differences in treatment decisionsthrough study completion, an average of 1 yearThe surgical rates of each patient will be assessed in each arm. Demographic variables will be controlled for especially race, ethnicity, socioeconomic variables.

Countries

United States

Contacts

Primary ContactAlison Saville, MSPH, MSW
alison.saville@cuanschutz.edu7202574406

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026