Effectiveness of a mHealth Intervention for the Treatment of Depression in People With Diabetes or Hypertension in Peru

NCT03026426 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 432

Last updated 2021-05-11

No results posted yet for this study

Summary

Background: Depression is a common comorbidity of physical chronic diseases such as diabetes and/or hypertension and constitutes an important public health problem. It correlates negatively with the patients' quality of life and self-care, as well as compliance with medical treatment. In low- and middle-income countries depression often goes unrecognized and untreated, and there are limited human resources to treat depression and other mental problems.

Aim: The present study aims to test a 6-week low-intensity psychological intervention (CONEMO - CONtrol EMOcional) delivered by a smartphone application to people with depressive symptoms and co-morbid diabetes and/or hypertension recruited in primary health care centers and public hospitals in Lima, Peru.

Conditions

Interventions

BEHAVIORAL

CONEMO

Participants will be offered a behavioral activation-based intervention delivered by an application for smartphones (CONEMO) oriented to encourage them to be more active and to incorporate more activities in participants' everyday life. Nurses will train participants to use CONEMO, make phone calls when participants are non-adherent, and provide technical support when necessary. Nurses will be supervised by clinical psychologists.

Sponsors & Collaborators

  • University of Sao Paulo General Hospital

    collaborator OTHER
  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • Northwestern University

    collaborator OTHER
  • Universidad Peruana Cayetano Heredia

    lead OTHER

Principal Investigators

  • Paulo R Menezes, MD, PhD · University of Sao Paulo General Hospital

  • Ricardo B Araya, MD, PhD · London School of Hygiene and Tropical Medicine

  • Jaime Miranda, MD, PhD · Universidad Peruana Cayetano Heredia

  • Lisa Colpe, PhD · National Institute of Mental Health (NIMH)

  • Francisco Diez-Canseco, MSc, MPH · Universidad Peruana Cayetano Heredia

  • Lena R Brandt, MSc · Universidad Peruana Cayetano Heredia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-24
Primary Completion
2018-03-31
Completion
2018-12-19

Countries

  • Peru

Study Locations

More Related Trials

Entities

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 NCT03026426 on ClinicalTrials.gov