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Clinical Trials/NCT05149417
NCT05149417
Completed
Not Applicable

Effect of Telemedecine on Post-trauma Pain Medication Adherence After Discharge From Emergency Departement

University of Monastir2 sites in 1 country1,350 target enrollmentAugust 21, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post-traumatic Pain
Sponsor
University of Monastir
Enrollment
1350
Locations
2
Primary Endpoint
Visual analog scale after 7 days of follow-up
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The impact of telemonitoring on patients' adherence to post trauma pain treatment , their satisfaction and pain relief after discharge from the ED.

Detailed Description

This is a prospective, multicenter, randomized trial . Participants are recruited from the emergency departement of Fattouma Bourguiba Monastir. This study is a seven day three-arm parallel group trial . Participants inculded are aged more than 16 years old who presented to the ED for minor trauma and discharged with analgesic treatment. They are randomized to one of two trial TM intervention groups (SMS and TM) or usual care group (control) in a 1 :1 :1 allocation ratio. For all inculded patients, demographic characteristics were collected as well as clinical examination findings. The interventional care provided at the ED was mentioned. At ED discharge the pain Visual Analogue Scale (VAS) was evaluated and the analgesic treatment prescribed was noted.

Registry
clinicaltrials.gov
Start Date
August 21, 2020
End Date
July 31, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pr. Semir Nouira

chief of the Emergency departement in CHU fattouma Bourguiba Monastir , PhD

University of Monastir

Eligibility Criteria

Inclusion Criteria

  • Age \>16 years old with minor trauma and discharged with an analgesic treatment.
  • Included patients should have regular access to a mobile phone ,were able to interact with SMS or could do so with help of a relative.
  • Patients who accepted to participate to the study.
  • No contraindication to analgesic medication

Exclusion Criteria

  • Swallowing disorder or inability to swallow.
  • Unsuitable for follow-up.

Outcomes

Primary Outcomes

Visual analog scale after 7 days of follow-up

Time Frame: at seven day after ED discharge .

Patient's adherence to analgesics treatment which was assessed by calling patients or by sending SMS in day 2, day 4,and day 7 in SMS group and the telemonitoring group respectively.

Secondary Outcomes

  • Likert scale(at seven day post ED discharge .)

Study Sites (2)

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