NCT01105923

Brief Summary

The aim of this study is to identify patients with problem list gaps and intervene to correct these gaps by creating clinical decision support interventions that alert providers to likely problem list gaps and offer clinicians the opportunity to correct them. The investigators will randomize the clinics that will receive the intervention and formally evaluate the study after a period of 6 months for improved problem list completeness to determine the effectiveness of our intervention.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
140

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2010

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 15, 2010

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 19, 2010

Completed
12 days until next milestone

Study Start

First participant enrolled

May 1, 2010

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2010

Completed
7 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2017

Completed
Last Updated

February 2, 2015

Status Verified

January 1, 2015

Enrollment Period

6 months

First QC Date

April 15, 2010

Last Update Submit

January 30, 2015

Conditions

Outcome Measures

Primary Outcomes (1)

  • Intervention acceptance

    Of those providers who were shown (or who would have been shown, for the control group) the intervention, the number that added a problem across control and intervention groups.

    6 months (May 2010-Nov2010)

Secondary Outcomes (3)

  • Problem list prevalence

    pre and post intervention

  • Problem list incidence

    pre and post intervention

  • Quality improvement based on problem list accuracy/completion

    post intervention

Study Arms (2)

Receive CDS intervention

EXPERIMENTAL

Providers in clinics that will receive the CDS alert, as their clinic was randomized into our study.

Other: MAPLE

No CDS intervention

NO INTERVENTION

Interventions

MAPLEOTHER

MAPLE is a CDS intervention within the EHR that will alert providers to problem lists gaps and present an opportunity to correct them.

Receive CDS intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Independent healthcare provider (physician, NP, PA)
  • Practices at participating site

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Brigham and Women's Hospital

Boston, Massachusetts, 02115, United States

Location

Related Publications (1)

  • Wright A, Pang J, Feblowitz JC, Maloney FL, Wilcox AR, McLoughlin KS, Ramelson H, Schneider L, Bates DW. Improving completeness of electronic problem lists through clinical decision support: a randomized, controlled trial. J Am Med Inform Assoc. 2012 Jul-Aug;19(4):555-61. doi: 10.1136/amiajnl-2011-000521. Epub 2012 Jan 3.

MeSH Terms

Conditions

Attention Deficit Disorder with HyperactivityAsthmaPulmonary Disease, Chronic ObstructiveBreast NeoplasmsCoronary Artery DiseaseHeart FailureDiabetes MellitusGlaucomaHemophilia AHypertensionHyperthyroidismHypothyroidismMyasthenia GravisOsteoporosisBone Diseases, MetabolicRenal InsufficiencyAnemia, Sickle CellStroke

Condition Hierarchy (Ancestors)

Attention Deficit and Disruptive Behavior DisordersNeurodevelopmental DisordersMental DisordersBronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesRespiratory HypersensitivityHypersensitivity, ImmediateHypersensitivityImmune System DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsNeoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesCoronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesArteriosclerosisArterial Occlusive DiseasesVascular DiseasesGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesOcular HypertensionEye DiseasesBlood Coagulation Disorders, InheritedBlood Coagulation DisordersHematologic DiseasesHemic and Lymphatic DiseasesCoagulation Protein DisordersHemorrhagic DisordersGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesThyroid DiseasesParaneoplastic Syndromes, Nervous SystemNervous System NeoplasmsParaneoplastic SyndromesAutoimmune Diseases of the Nervous SystemNervous System DiseasesNeurodegenerative DiseasesNeuromuscular Junction DiseasesNeuromuscular DiseasesAutoimmune DiseasesBone DiseasesMusculoskeletal DiseasesKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesAnemia, Hemolytic, CongenitalAnemia, HemolyticAnemiaHemoglobinopathiesCerebrovascular DisordersBrain DiseasesCentral Nervous System Diseases

Study Officials

  • Adam Wright, PhD

    Brigham and Women's Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior Scientist

Study Record Dates

First Submitted

April 15, 2010

First Posted

April 19, 2010

Study Start

May 1, 2010

Primary Completion

November 1, 2010

Study Completion

November 1, 2017

Last Updated

February 2, 2015

Record last verified: 2015-01

Locations