sábado, 17 de septiembre de 2016

A randomized controlled trial studying the effectiveness of group medical appointments on self-efficacy and adherence in sickle cell disease (TEAM study): study protocol | BMC Hematology | Full Text

A randomized controlled trial studying the effectiveness of group medical appointments on self-efficacy and adherence in sickle cell disease (TEAM study): study protocol | BMC Hematology | Full Text

Biomed Central

A randomized controlled trial studying the effectiveness of group medical appointments on self-efficacy and adherence in sickle cell disease (TEAM study): study protocol

  • Marlous J. Madderom,
  • Jessica Heijdra,
  • Elisabeth M. W. J. Utens,
  • Suzanne Polinder,
  • Anita W. Rijneveld and
  • Marjon H. CnossenEmail author
BMC HematologyBMC series – open, inclusive and trusted201616:21
DOI: 10.1186/s12878-016-0058-4
Received: 28 January 2015
Accepted: 16 June 2016
Published: 4 August 2016

Abstract

Background

Sickle cell disease (SCD) is endemic in non-Western countries. Due to migration, the prevalence of SCD in the Netherlands has increased. Adherence to medical treatment is recognized as a major problem area. Therefore, new effective interventions to increase adherence are urgently needed.

Methods/design

The TEAM study is an ongoing randomized controlled trial (RCT) to compare protocolized individual medical appointments (IMA’s; care-as-usual) with protocolized group medical appointments (GMA’s; novel intervention) in pediatric (n = 40) and adult (n = 60) patients. The study aims to assess the effectiveness of GMA’s (over a three year period) on patients’ self-efficacy, adherence, quality of life, morbidity, hospital admissions and satisfaction with the treating professional; as well as to test the cost-effectiveness of GMA’s. In both the IMA and GMA groups structured assessments will be performed at baseline (start of the study), after 1.5 and after 3 years.

Discussion

This is the first RCT to investigate the effectiveness of GMA’s on self-efficacy and adherence in pediatric and adult patients with SCD, including a cost-effectiveness analysis.

Trial registration

NTR4750 (NL42182.000.12). Registered 13 August 2014.

Keywords

Randomized controlled trial Sickle cell disease Self-efficacy Adherence Group medical appointment Cost-effectiveness

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