Skip to main content
Clinical Trials/NCT04168554
NCT04168554
Unknown
N/A

Pilotonderzoek Naar Het Gebruik Van Telemedicine Bij Het Beoordelen Van Het Benauwde Kind in de Huisartsenpraktijk English: The Use of Telemedicine in the General Practitioners Office for a Child With Respiratory Symptoms: a Pilot Study

Rijnstate Hospital0 sites40 target enrollmentDecember 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Respiratory Distress Syndrome
Sponsor
Rijnstate Hospital
Enrollment
40
Primary Endpoint
Discharge or admitted?
Last Updated
6 years ago

Overview

Brief Summary

Pediatrician does physical examination through telemedicine and in real life to see whether the telemedicine consultation corresponds with the real life examination.

Goal is to determine:

  1. Check practical feasability
  2. Check whether there are no great objections for a larger study (ie. in case telemedicine consultation is much more unreliable to do a physical examination a larger study is deemed unsafe)

Detailed Description

40 pediatric patients seen by a general practitioner (GP) whom the GP has referred or wants to refer to a pediatrician for clinical evaluation are included in this study. Study is designed in 2 parts. Part 1 is at the emergency room in the hospital Part 2 is at the GPs office The pediatrician sees the patient through a telemedicine consultation. Then sees the patient in real life to see if what was seen during telemedicine corresponds with the real life consultation. With telemedicine and real life consultation the pediatrician rates the patient as either a candidate to go home or to be admitted. With the telemedicine consultation there is also an option "in doubt: i want to see the patient in real life". Also with both telemedicine and real life examination the pediatrician scores the patient using the respiratory observation scale (Siew et al, 2016) Goal is to: 1. Check practical feasability 2. Check whether there are no great objections for a larger study (ie. in case telemedicine consultation is much harder to do a physical examination

Registry
clinicaltrials.gov
Start Date
December 2019
End Date
November 2020
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Rijnstate Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Pediatric patients with respiratory symptoms whom are referred by a general practitioner to be evaluated by a pediatrician

Exclusion Criteria

  • Infants younger than 2 months of age
  • 19 years and older
  • Ex-premature with post-conceptional age \<48 weeks
  • Congenital heart disease
  • Down Syndrome
  • Immune deficiency
  • Pre-existent pulmonary disorder (Broncho-pulmonary dysplasia, Cystic Fibrosis)
  • Pre-existent neurological disorders
  • Patients with respiratory distress with dehydration symptoms
  • Patients who have already been treated with salbutamol inhalers of nebulizer - Emergency patient with respiratory insufficiency

Outcomes

Primary Outcomes

Discharge or admitted?

Time Frame: within 30-60 minutes after inclusion

Patients are categorized in one of three categories through telemedicine-evaluation Group 1: "Patient can safely go home" Group 2: "Patient will need to be admitted" Group 3: "In doubt between group 1 and group 2, emergency room consultation required" FTF evaluation: Group 1: "Patient can safely go home" Group 2: "Patient will need to be admitted"

Respiratory Observation Scale

Time Frame: within 30-60 minutes after inclusion

Observe the presence of: tachypnea, nasal flaring, perioral cyanosis, tripoding, thoracoabdominal asynchrony, supraclavicular-, substernal- or intercostal retractions, mental status and patient in respiratory distress

Secondary Outcomes

  • Patient reported experience measure(within 60 minutes after telemedicine evaluation)
  • Doctor reported experience measure(within 4 weeks after inclusion of patients)

Similar Trials