CClinicalTrials.gg
CompletedNCT02625129Updated Jan 19, 2018

Effectiveness of and Satisfaction With a Pharmacist-managed Travel Medicine Clinic

An observational study in Travel Medicine, sponsored by University of Waterloo. Completed at 1 site in Canada. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-01-19.

Sponsored by University of Waterloo · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
103
Ages
18 Years and older
Sex
All
01

Study summary

This study will evaluate the clinical effectiveness of, and patient satisfaction with, pre-travel consultations provided by a pharmacist with specialty training in travel medicine and the authorization to prescribe medications and administer vaccinations.

Read the detailed description

The study will be conducted at the Travel Health Network, a full-service travel medicine clinic located in St. Albert, Alberta. Care will be provided by a pharmacist with a specialized practice in travel medicine, authorization to prescribe vaccines and prescription drugs, and authorization to administer vaccines by injection.

The study will be a prospective mixed-methods cohort study, describing patients receiving care from a pharmacist-managed travel medicine clinic and their travel health needs, and evaluating their adherence to recommended vaccines and oral therapies, satisfaction with the care provided, and their health status and management of health issues arising while travelling. Chart reviews will elicit descriptive quantitative data related to patients' travel medicine needs and adherence to recommended vaccinations and oral pharmacotherapy, followed by surveys containing open-ended qualitative questions to elicit overall patient satisfaction and the management of any health issues encountered during travel. Due to the nature of the study involving patients presenting to the clinic for a consultation, neither a control group nor blinding is possible.

A convenience sample of 100 subjects will be enrolled.

02

Conditions studied

  • Travel Medicine
03

In context

Lead sponsor

University of Waterloo is the lead sponsor of 90 studies on the registry; 8 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 9 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population will consist of individuals presenting for travel consultations at the Travel Health Network. No restrictions will be placed related to patient demographics, destinations, or travel itineraries; however, travellers with an expected return date after September 1, 2016 will be excluded, to ensure complete follow-up and data analysis within the proposed project time frame. A convenience sample of 100 patients will be consecutively enrolled .

Inclusion criteria

  • Receiving a pre-travel consultation at the Travel Health Network clinic in St. Albert, Alberta, Canada

Exclusion criteria

Exclusion Criteria:

  • Travellers with an expected return date after September 1, 2016
  • Those receiving consultations as part of a group with the same itinerary (e.g., families, group vacations) will be asked to identify one member to participate in order to minimize repetition among participants.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
103 participants (actual)
Patient registry
No

Groups and cohorts

  • Pharmacist-provided travel care

    Other: Pharmacist-provided travel care

Interventions

  • OtherPharmacist-provided travel care

    Subjects will receive a pre-travel consultation from a pharmacist with specialty training in travel medicine, and with authorization to prescribe medications and vaccines and administer injections

06

What researchers measure

Primary outcomes

  1. The proportion of recommended pre-travel vaccinations administered before departure according to chart review

    From date of pre-travel consultation until the date of travel departure according to participant's planned itinerary, assessed up to September 2016.

    Time frame: Up to 7 months.

  2. The proportion of recommended pre-travel oral pharmacotherapies dispensed before departure by a community pharmacy according to electronic health record

    From date of pre-travel consultation until the date of travel departure according to participant's planned itinerary, assessed up to September 2016.

    Time frame: Up to 7 months.

Secondary outcomes

  1. Average satisfaction (along 1-5 scale) with care provided elicited through an online survey post-travel

    Time frame: 1 week following return from travel according to participant's planned itinerary

  2. Frequency of reason(s) for declining any recommended vaccines or medications according to participant self-report through an online survey

    Response options: didn't feel I was at risk, cost, concern about vaccine ingredients or safety, other (specify)

    Time frame: 1 week following return from travel according to participant's planned itinerary

  3. Number of reports of any health issues over the course of travel according to participant self-report through an online survey

    Response options: Traveller's diarrhea, Altitude sickness, Malaria, Fever (Dengue, Chikungunya), Respiratory illness, Other (specify)

    Time frame: 1 week following return from travel according to participant's planned itinerary

  4. Frequency of management strategies of any health issues over the course of travel according to participant self-report through an online survey

    Response options: Nothing - it went away on its own, Took a non-prescription medication I had purchased before departure, Took a non-prescription medication I purchased while travelling, Called or emailed the Travel Health Network for advice, Searched the internet for guidance on how to manage it, Saw a physician while travelling, Saw a physician upon returning home, Other (specify)

    Time frame: 1 week following return from travel according to participant's planned itinerary

07

Study locations

1 site
  • Travel Health Network
    St. Albert, Alberta T8N5H9, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 19, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02625129
Lead sponsor
University of Waterloo
Collaborators
University of Mississippi Medical Center, Travel Health Network
Responsible party
Sponsor
First posted
Dec 9, 2015
Start date
Feb 2016
Primary completion
Apr 2017
Completion
Apr 2017
Last update
Jan 19, 2018

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion