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Child Health Improvement Through Computer Automation (CHICA) Highlighting Study

Increasing Prompt Response Rates in the CHICA System

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01583101
Enrollment
2237
Registered
2012-04-23
Start date
2012-04-30
Completion date
2012-10-31
Last updated
2017-05-15

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

Conditions

Physician Behavior

Brief summary

The investigators have developed a novel decision support system for implementing clinical guidelines in pediatric practice. CHICA (Child Health Improvement through Computer Automation) combines three elements: (1) pediatric guidelines encoded in Arden Syntax; (2) a dynamic, scannable paper user interface; and (3) an HL7-compliant interface to existing electronic medical record systems. The result is a system that both delivers just-in-time patient-relevant guidelines to physicians during the clinical encounter, and accurately captures structured data from all who interact with it. Preliminary work with CHICA has demonstrated the feasibility of using the system to implement and evaluate clinical guidelines. However, analyses have shown that physicians ignore a fair number of prompts. The investigators would like to experiment with changes to the system to see if they can increase physicians' response rates. This could include highlighting prompts, reordering them, or flagging them in other ways. The main outcome of interest in the rate at which physicians answer prompts.

Detailed description

We have developed a novel decision support system for implementing clinical guidelines in pediatric practice. CHICA (Child Health Improvement through Computer Automation) combines three elements: (1) pediatric guidelines encoded in Arden Syntax; (2) a dynamic, scannable paper user interface; and (3) an HL7-compliant interface to existing electronic medical record systems. The result is a system that both delivers just-in-time patient-relevant guidelines to physicians during the clinical encounter, and accurately captures structured data from all who interact with it. Preliminary work with CHICA has demonstrated the feasibility of using the system to implement and evaluate clinical guidelines. However, analyses have shown that physicians ignore a fair number of prompts. We would like to experiment with changes to the system to see if we can increase physicians' response rates. This could include highlighting prompts, reordering them, or flagging them in other ways. The main outcome of interest is the rate at which physicians answer prompts. This will be a randomized, controlled trial of the CHICA system to see if we can improve prompt response rates. We will randomize physicians or clinics to receive some form of prompt change, including highlighting them, reordering them, or flagging them. No other changes will be made to care. We will extract data from the CHICA system for all patients seen in our study clinics. This data will include a the clinic location, whether or not a physician responded to a prompt, the prompt's position on the form, the patient's gender, the rule priority of the prompt, rule title, patient insurance category, the patient's age in days, and the name of the provider. The main outcome of interest is whether or not a prompt was answered (discussed/not discussed).

Interventions

OTHERReceiving Highlighted Prompts

Prompts received by physicians were highlighted.

OTHERReceiving Non-highlighted Prompts

Prompts received by physicians were not highlighted.

Sponsors

Indiana University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Physicians practicing in one of our four CHICA clinics who use CHICA

Exclusion criteria

* Not being a physician practicing in one of our four CHICA clinics who use CHICA

Design outcomes

Primary

MeasureTime frameDescription
The Number of Prompts That Were Responded to1 yearThe main outcome of interest is whether or not a prompt was answered (discussed/not discussed).

Countries

United States

Participant flow

Pre-assignment details

While physicians were the ones that received prompts, the prompts are the unit of analysis.

Participants by arm

ArmCount
Receiving Highlighted Prompts
These patients received highlighted prompts.
1,076
Receiving Non-highlighted Prompts
These patients received prompts that were not highlighted.
1,161
Total2,237

Baseline characteristics

CharacteristicReceiving Highlighted PromptsReceiving Non-highlighted PromptsTotal
Age, Categorical
<=18 years
1076 Participants1161 Participants2237 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
0 Participants0 Participants0 Participants
Sex/Gender, Customized
Unknown
1076 Participants1161 Participants2237 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 1,0760 / 1,161
serious
Total, serious adverse events
0 / 1,0760 / 1,161

Outcome results

Primary

The Number of Prompts That Were Responded to

The main outcome of interest is whether or not a prompt was answered (discussed/not discussed).

Time frame: 1 year

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Receiving Highlighted PromptsThe Number of Prompts That Were Responded to672 Participants
Receiving Non-highlighted PromptsThe Number of Prompts That Were Responded to712 Participants

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