The Use of Educational Technology in Improving Adherence Therapy

NCT03324386 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 57

Last updated 2017-10-27

No results posted yet for this study

Summary

Few studies show the benefits of educational technologies a support for the control of chronic diseases. The approach known as 'embracement' adopts relational strategies or soft technologies which promote bonding and may impact therapy adherence and quality of life in hypertensive patients.Objectives:To assess the impact of the embracement approach on therapy adherence, quality of life, and the white coat effect in hypertensive outpatients followed in a specialized clinic. This approach may be associated or not with the use of educational technology in a virtual learning environment(VLE) for distance learning (DL) and with use the educational technology in Blended E-learning (E-BLENDED)

Conditions

  • Medication Nonadherence
  • Hypertension, Resistant to Conventional Therapy

Interventions

BEHAVIORAL

Experimental: Individual Orientation

This approach may be individual orientation with by an embracement strategy (relational strategies) may be making 7 nursing visits at 20-day intervals, for 4 month.

BEHAVIORAL

Experimental: VLE for Distance Learning

Experimental: This approach may be associated with the use of educational technology (E-Care of Hypertension) in a virtual learning environment(VLE) for distance learning (DL) consultation with the health professional and making 7 nursing visits at 20-day intervals, for 4 months

BEHAVIORAL

Experimental: E-blended Lerarning

This approach may be associated with the use of educational technology (E-Care of Hypertension) in the blended e-learning mode associated with face-to-face with the health professional and making 7 nursing visits at 20-day intervals, for 4 months

OTHER

Conventional Therapy - Control Group

This approach may be individual orientation with conventional therapy may be making 2 nursing visits at baseline and 1 after 120 days,

Sponsors & Collaborators

  • Luiz Aparecido Bortolotto

    collaborator UNKNOWN
  • Chao Lung Wen

    collaborator UNKNOWN
  • Margarida Vieira

    collaborator UNKNOWN
  • Miriam Harume Tsunemi

    collaborator UNKNOWN
  • Isabela Ribeiro Braga Fistarol

    collaborator UNKNOWN
  • Jefferson Carlos de Oliveira

    collaborator UNKNOWN
  • Dante Marcelo Artiga Giorgi

    collaborator UNKNOWN
  • Heno Ferreira Lopes

    collaborator UNKNOWN
  • Fernanda Marciano Consolim-Colombo

    collaborator UNKNOWN
  • Ivonete Sanches Giacometti Kowalski

    collaborator UNKNOWN
  • University of Sao Paulo General Hospital

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-18
Primary Completion
2015-04-25
Completion
2017-02-17

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03324386 on ClinicalTrials.gov