NCT03354000

Brief Summary

Online patient portals are becoming ubiquitous in the US. Previous research has documented substantial usability barriers, especially among patients with limited health literacy. This pilot randomized pilot trial had the goal of determining the effectiveness of an in-person training with a scalable online video-based training program to increase portal use among patients in a safety net healthcare setting.

Trial Health

100
On Track

Trial Health Score

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

Enrollment
93

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2015

Typical duration for not_applicable

Status
completed

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

August 1, 2015

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2017

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

November 9, 2017

Completed
18 days until next milestone

First Posted

Study publicly available on registry

November 27, 2017

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2018

Completed
Last Updated

April 19, 2019

Status Verified

April 1, 2019

Enrollment Period

2 years

First QC Date

November 9, 2017

Last Update Submit

April 17, 2019

Conditions

Keywords

Patient PortalHealthcare disparitiesSafety net healthcare system

Outcome Measures

Primary Outcomes (1)

  • Portal log-ins

    Logging into the portal website in the 3-6 months post-training (yes/no)

    3-6 months post-training

Secondary Outcomes (3)

  • eHealth Literacy

    3-6 months post-training

  • Portal sign-up

    3-6 months post-training

  • Digital literacy skills

    3-6 months post-training

Study Arms (2)

Take-home online training

PLACEBO COMPARATOR

Participants received a link to access the online tutorial videos on their own.

Behavioral: Take-home online training

In-person online training

ACTIVE COMPARATOR

Participants received an in-person tutorial of how to use the patient portal website with a trained research assistant.

Behavioral: In-person online training

Interventions

We randomized patients to receive a link to access the online tutorial on their own. Participants in the take-home arm were given a paper handout with a link to the training materials and an outline of the steps for accessing the training curriculum.

Take-home online training

For participants randomized to the in-person training arm, a trained research assistant prompted participants to log into the learning platform and guided them in accessing the training materials for portal features that were of interest to them. The staff member provided further explanation or clarification if participants had questions about the training material.

In-person online training

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • English-speaking as portal is only available in English
  • diagnosed with at least one chronic condition

You may not qualify if:

  • cognitive impairment
  • visual impairment
  • severe mental health conditions
  • any circumstances that would make participation in the study difficult
  • no previous email use
  • self-reported usage of MYSFHEALTH

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Norman CD, Skinner HA. eHEALS: The eHealth Literacy Scale. J Med Internet Res. 2006 Nov 14;8(4):e27. doi: 10.2196/jmir.8.4.e27.

    PMID: 17213046BACKGROUND

Related Links

MeSH Terms

Conditions

Chronic Disease

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Courtney Lyles, PhD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

November 9, 2017

First Posted

November 27, 2017

Study Start

August 1, 2015

Primary Completion

July 31, 2017

Study Completion

July 31, 2018

Last Updated

April 19, 2019

Record last verified: 2019-04