Filter Paper Blood Spots Collected During Fever as a Source for Post-travel Diagnosis in Travelers

Fever Clinical Trial

— JOKA-II  

Official title:

Filter Paper Blood Spots Collected During Fever as a Source for Post-travel Diagnosis of Arboviral and Rickettsial Infections in a Cohort of Travelers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02900066
• Other study ID #: B-300201627244
• Status: Completed
• Start date: February 1, 2016
• Est. completion date: September 1, 2018

Study information

• Verified date: March 2021
• Source: Institute of Tropical Medicine, Belgium
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

This study is part of a larger prospective cohort study (JOKA), designed to study febrile illness occurring during a travel to the tropics, as well as the evaluation of the clinical use of malaria rapid diagnostic tests (RDT) by travelers or their peers during travel, as a decision aid for the management of febrile illness in the tropics.

Filter paper blood spots and paired serology are used in addition to routine post-travel evaluation, to study the incidence and etiological spectrum of febrile illness occurring during travel to the tropics.

The study will yield valuable and prospective data of incidence rate, the clinical and etiological spectrum, clinical course and outcome of febrile illness during (and post-)travel in a prospective cohorts of travelers. This knowledge may lead to better pre-travel advice.

Description:

Objectives:

To study the incidence etiological spectrum of febrile illness occurring during a travel to the tropics, as well as clinical course, care, treatment and outcome of these febrile illness episodes.

Design: Prospective cohort study of febrile illness in international travelers Population:

Travelers who are going to destinations in the tropics (South-East Asia (SEA), Sub-Saharan Africa (SSA) and South America (SCA)) for 3 weeks or longer will be invited to participate and, after obtaining informed consent, recruited in the study protocol(s) at the time of planning departure (directly at the ITM or through travel/ humanitarian relief organizations).

Methods:

Participants will be offered pre-, per- and post-travel consultation as explained below (Inclusion through ITM)

1. Pre-travel consultation at a certified travel clinic will systematically be recommended; this consultation will include:

1. routine travel advice directed at travel destination, (including vaccinations and prescription for anti-malarial chemoprophylaxis according to current recommendations, details of which are published at www.reisgeneeskunde.be and

2. the following research-related activities.

• Briefing sessions on the topic "Fever in The Tropics" by an ITM physician (during this session the differences between fever at home and in the tropics will be addressed and the importance of consulting a local doctor will be stressed).

• Collection and recording of demographic, clinical and travel data.

• Sampling of a baseline serum sample (for paired pre- and post-travel diagnostic analysis).

• Training of travelers, peers and travel guides to blot capillary blood on a filter paper (training is a prerequisite for study participation).

• Provision of study materials (study diary/apps, malaria kits, thermometer, …) and written instructions for use during travel if fever occurs (see below)

2. During travel

• In case of any illness (associated with fever or not), the traveler will record symptoms in the study diary.

• If fever is documented (axillary temperature ≥ 37.8°C - or in case a thermometer is not immediately available, fever sensation in association with sweats or chills)- blood from a finger prick will be collected for blotting onto filter paper (BFP) by trained travelers or peers.

• All febrile travelers are advised to seek medical attendance as they would do when not participating in the study.

• The final decision to use standby emergency treatment malaria treatment (SBET) is made by the study participant, in accordance with precise and written instructions.

• The study team (Tropical medicine experts at ITM) will be available for teleconsultation by Email or Telephone, and will provide medical advice within 12 hours. Note: contacting the ITM study team is an option, but should not cause delay in treating suspected malaria.

• Study participants will collect all relevant data related to the (outcome of the) illness episode (duration of symptoms, consultation of a health practitioner, admission/duration of stay in a hospital, treatment received and timing, repatriation)

3. Post-travel consultation will be scheduled for all study participants who experience(d) any illness (febrile or not) within a week after travel- sooner if the medical condition requires so- and for those who have no complaints but do seek post-travel health evaluation.

• A structured clinical evaluation will be performed by an expert in travel medicine and will be recorded in the database. Laboratory evaluation will include hematological, biochemical and microbiological/parasitological analysis

• Used BFPs (i.e. in case of febrile illness during travel) will be collected for confirmation of the test result by Polymerase Chain Reaction (PCR). A diagnostic protocol/ algorithm will be developed for use the BFPs as a source for post-travel diagnosis of arboviral/ rickettsial infection by PCR.

• Data analysis : All data (demographic, geographic, clinical, laboratory and final diagnosis) will be recorded in an encoded database. Descriptive and inferential statistics as appropriate, STATA 14.

• Sample size: n= 350 fever cases; at an incidence of fever of 8% a cohort of 4400 (healthy) travelers will be recruited over 30 months (Feb 2016 - Aug 2018).

• Endpoints:

• Incidence rates for malaria and arboviral/ rickettsial infections (by paired serology and post-travel PCR on BFP) per travel destination.

• Clinical course and outcomes of (self-)management of febrile illness during travel. (Clinical spectrum of disease, incidence rates of febrile illnesses; duration of fever and other symptoms, management (self-treatment, consultation, admission), type of treatment (symptomatic/empiric/targeted if RDT malaria positive), final outcome (change of travel plans, repatriation, hospitalization as a result of illness during travel).

Expected results and relevance: The study will yield valuable and prospective data of incidence rate, the clinical and etiological spectrum, clinical course and outcome of febrile illness during (and post-)travel in a prospective cohorts of travelers. This knowledge may lead to better pre-travel advice.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 350
• Est. completion date: September 1, 2018
• Est. primary completion date: December 1, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Residing in Belgium.

• Attend a briefing session on the topic "Fever in The Tropics" by an ITM physician.

• Able to comply with study procedures:

• Carry and complete a study diary in case of illness

• Be trained to collect BFP OR

• Travel with anyone who has been trained

• Willing and able to provide written informed consent.

• Adults fulfilling all criteria and volunteer to have their BFP collected by their trained peers during travel, may be included for analysis after obtaining informed consent upon post-travel evaluation.

Exclusion criteria:

• Unable to comply with study protocol.

Related Conditions & MeSH terms

• Fever

Locations

Country	Name	City	State
Belgium	ITM	Antwerp

Sponsors (1)

Lead Sponsor	Collaborator
Institute of Tropical Medicine, Belgium

Country where clinical trial is conducted

Belgium, 

References & Publications (1)

Huits R, Van Den Bossche D, Eggermont K, Lotgering E, Feyens AM, Potters I, Jacobs J, Van Esbroeck M, Cnops L, Bottieau E. Incidence of Zika virus infection in a prospective cohort of Belgian travellers to the Americas in 2016. Int J Infect Dis. 2019 Jan; — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of etiological diagnoses in febrile travelers as assessed by post hoc clinical evaluation	PCR analysis will be directed by antibody detection in paired sera, and post-travel clinical evaluation	up to 6 months of follow-up per individual traveler
Secondary	Clinical outcome of febrile illness during travel	Final clinical outcome per diagnosis (change of travel plans, repatriation, hospitalization as a result of illness during travel, death).	up to 6 months of follow-up per individual traveler
Secondary	incidence of etiological diagnoses of fever expressed as risk per person- year of travel per region traveled		up to 6 months of follow-up per individual traveler
Secondary	Time from start of travel to development of fever by self-reporting		up to 6 months of follow-up per individual traveler
Secondary	duration of symptoms by self-reporting in a structured study diary		up to 6 months of follow-up per individual traveler
Secondary	Type of treatment per diagnosis reported in a structured study diary	symptomatic/ empiric/ targeted upon diagnosis abroad	up to 6 months of follow-up per individual traveler