NCT03224078

Brief Summary

The overall aim of INDEED is to facilitate trans-sectoral and interdisciplinary health services research of emergency care in Germany. Clinical hospital data from 15 to 20 emergency departments in Germany will be linked to routine ambulatory health care data provided by the Association of Statutory Health Insurance Physicians (Kassenärztliche Vereinigung, KV). INDEED will identify health care gaps and inadequate resource allocation as well as develop strategies for adaptations of the health care system to existing demands.

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
680,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2017

Typical duration for all trials

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2017

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

June 23, 2017

Completed
28 days until next milestone

First Posted

Study publicly available on registry

July 21, 2017

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2020

Completed
Last Updated

July 21, 2017

Status Verified

July 1, 2017

Enrollment Period

3 years

First QC Date

June 23, 2017

Last Update Submit

July 19, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • Prevalence of adequate, inadequate and avoidable ED-visits

    Prevalence of adequate, inadequate and avoidable ED-visits will be operationalized by a) patients with low utilization of primary health care, b) low urgency, c) preventable conditions, d) chronic diseases that could have been adequately controlled, e) frequent-users, f) patients without contact to a physician in the ED ("left without being seen").

    Baseline

Secondary Outcomes (7)

  • Characterization of health care resource utilization before and after an ED-visit

    from 2 years before until 1 year after ED-visit (2014-2017)

  • influencing factors on avoidable ED-visits

    from 2 years before until 1 year after ED-visit (2014-2017)

  • influencing factors on adequate ED-visits

    from 2 years before until 1 year after ED-visit (2014-2017)

  • influencing factors on inadequate ED-visits

    from 2 years before until 1 year after ED-visit (2014-2017)

  • Exploratory analysis of influencing factors on increased health care costs.

    from 2 years before until 1 year after ED-visit (2014-2017)

  • +2 more secondary outcomes

Study Arms (1)

adult Emergency Department Patients

adult patients that were treated with any condition in one of the participating emergency departments in 2016 (n≈680.000 cases)

Other: data extraction

Interventions

No Special interventions except from data extraction form the respective routine data sources are planned .

adult Emergency Department Patients

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients with public health insurance who attended one of the participating EDs in 2016 will be included in this research Project.

You may qualify if:

  • adult ED patients who attended one of the participating EDs in 2016
  • patients with public health insurance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Charité Universitätsmedizin - Berlin

Berlin, 13353, Germany

RECRUITING

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Martin Möckel, Prof. Dr.

    Charite University, Berlin, Germany

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Martin Möckel, Prof. Dr.

CONTACT

Anna Slagman, Dr., MSc

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr.

Study Record Dates

First Submitted

June 23, 2017

First Posted

July 21, 2017

Study Start

May 1, 2017

Primary Completion

April 30, 2020

Study Completion

April 30, 2020

Last Updated

July 21, 2017

Record last verified: 2017-07

Data Sharing

IPD Sharing
Will not share

Individual participant data could be made available to other researchers on reasonable request and if data protection requirements are met.

Locations