Automated System for Gathering and Reporting Clinical Out... | NCT02453074

Studies
Automated System for Gathering and Reporting Clinical Outcomes to Providers

NCT02453074

Sponsor

Harvard Medical School (HMS and HSDM)

Status

Completed

Last Update Posted

May 25, 2015Estimated

Enrollment

326Actual

Phase

Not provided

Conditions

Ambulatory Care

Interventions

Online survey - Follow up for Better Care

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

May 2015

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 2015

Primary Completion Date

Feb 2015Actual

Completion Date

Apr 2015Actual

First Submitted Date

May 21, 2015

First Submission Date that Met QC Criteria

May 21, 2015

First Posted Date

May 25, 2015Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

May 21, 2015

Last Update Posted Date

May 25, 2015Estimated

Sponsor/Collaborators Module

Responsible Party, by Official Title

Ben Gross, Ben Gross, Harvard Medical School (HMS and HSDM)Principal Investigator

Lead Sponsor

Harvard Medical School (HMS and HSDM)OTHER

Collaborators

Not provided

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Not provided

Is FDA Regulated Device

Not provided

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

The purpose of this study is to design and test the feasibility of a system to survey patients regarding the outcome of acute care visits and to report back to the healthcare providers.

Detailed Description

Not provided

Design Module

Study Type

Observational

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Target Follow-Up Duration

Not provided

Phases

Not provided

Interventional Study Design

Allocation

Not provided

Intervention Model

Biospecimen

No data available

No data is available for this block.

Enrollment

326Actual

Name	Type	Description	Arm Group Labels	Other Names
Online survey - Follow up for Better Care	Other

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Survey response rate		Assessed at the end of the 12 week study period

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Adults age 18 and older visiting participating primary care clinics who agree to be contacted by email to complete a survey on clinical outcomes.

Exclusion Criteria:

None

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

Not provided

Standard Ages

AdultOlder Adult

Study Population

Patients of two primary clinics at Massachusetts General Hospital, Boston MA

Sampling Method

Non-Probability Sample