NCT02393534

Brief Summary

Doctors frequently speak with their patients over the telephone. Having a visit with a doctor over the telephone rather than face-to-face can be convenient for patients and allow them to save time and money on transportation and missed time from work. However, some patients may prefer seeing the doctor in person. In this study, we will study two groups of patients - some who have their visits with their doctor over the telephone and some who have them face-to-face. Using surveys and interviews, we will study if the groups differ in their satisfaction with their visit with their doctor after participating in the study for 6 months. We will also look at doctor satisfaction with telephone visits, use of clinic resources and if patients received recommended care such as laboratory tests and vaccines during the study period.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
11

participants targeted

Target at below P25 for phase_4

Timeline
Completed

Started Jun 2015

Shorter than P25 for phase_4

Geographic Reach
1 country

1 active site

Status
completed

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

March 9, 2015

Completed
10 days until next milestone

First Posted

Study publicly available on registry

March 19, 2015

Completed
2 months until next milestone

Study Start

First participant enrolled

June 1, 2015

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2016

Completed
Last Updated

April 6, 2016

Status Verified

April 1, 2016

Enrollment Period

10 months

First QC Date

March 9, 2015

Last Update Submit

April 5, 2016

Conditions

Keywords

Primary CareHealth Services ResearchTelemedicine

Outcome Measures

Primary Outcomes (1)

  • Feasibility assessment

    Proportion of patients recruited out of the total population and proportion of patients retained at 6 months.

    6 months

Secondary Outcomes (3)

  • Provider workload

    6 months

  • Provider workload

    6 months

  • Patient Satisfaction

    6 months

Other Outcomes (2)

  • Provider Satisfaction

    6 months

  • Patient receipt of medical recommendations

    6 months

Study Arms (2)

Usual Care

NO INTERVENTION

Eligible patients that are randomized to the usual care arm will have a standard in-person clinic visit with their primary care provider.

Telephone visit

EXPERIMENTAL

Eligible patients that are randomized to the telephone follow-up arm will have their next medical visit with their primary care provider via a telephone call.

Other: Telephone Visit

Interventions

Eligible patients that are randomized to the telephone follow-up arm will have their next medical visit with their primary care provider via a telephone call.

Telephone visit

Eligibility Criteria

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

You may qualify if:

  • Have a follow-up issue that can be addressed over the phone (as determined by their provider);
  • years of age or older;
  • Have a working telephone number; and
  • Are English, Spanish, Cantonese or Mandarin-speaking.

You may not qualify if:

  • Patient refusal or are unable to provide informed consent;
  • Currently participate in another clinical trial;
  • Have significant psychiatric comorbidity or cognitive impairment that would compromise their ability to participate (as determined by their provider); or
  • Plan to discontinue care at the Gouverneur Ambulatory Care Practice within the next 6 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gouverneur TDC

New York, New York, 10002, United States

Location

Study Officials

  • Antoinette Schoenthaler

    NYU School of Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 4
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 9, 2015

First Posted

March 19, 2015

Study Start

June 1, 2015

Primary Completion

April 1, 2016

Study Completion

April 1, 2016

Last Updated

April 6, 2016

Record last verified: 2016-04

Locations