MedPath

Acupuncture for Infectious Mononucleosis Trial

Phase 2
Terminated
Conditions
Infectious Mononucleosis
Interventions
Other: standard medical care
Procedure: traditional Chinese acupuncture
Registration Number
NCT00598988
Lead Sponsor
University of Alberta
Brief Summary

The purpose of this study is to investigate feasibility issues related to conducting an acupuncture study in a population of adolescents and young adults with infectious mononucleosis. Additionally, this study will provide preliminary data regarding treatment parameters (acupuncture and standard care) and outcomes (i.e. fatigue).

Detailed Description

This study examines the feasibility of treating adolescents and young adults diagnosed with infectious mononucleosis with acupuncture. Additionally, this study will provide preliminary data regarding treatment parameters (acupuncture and standard care) and outcomes (i.e. fatigue).

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
3
Inclusion Criteria
  • mono diagnosis confirmed by lab test
  • 21 days or less between start of symptoms and diagnostic test
  • presence of fatigue of at least 4/11 (by Chalder Fatigue Questionnaire)
  • no other illnesses present
  • meets residency requirement
Exclusion Criteria
  • insufficient communication in English
  • unable to begin acupuncture within 21 days of diagnostic test
  • acupuncture use currently or in the preceding 3 months
  • currently under the care of a TCM practitioner
  • unwilling to be randomized

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard medical carestandard medical carestandard medical care
Acupuncturetraditional Chinese acupunctureTraditional Chinese acupuncture in conjunction with standard medical care
Primary Outcome Measures
NameTimeMethod
Chalder Fatigue Questionnaire12 weeks
Secondary Outcome Measures
NameTimeMethod
MOS SF-3612 weeks

Trial Locations

Locations (1)

University of Alberta

🇨🇦

Edmonton, Alberta, Canada

© Copyright 2025. All Rights Reserved by MedPath