A Mobile App to Improve Participation in Following-up Cohorts

NCT04714788 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 310

Last updated 2021-01-19

No results posted yet for this study

Summary

The main objective is to test the superiority of a newly developed mobile application - RECAP\_MyLife - for data collection in cohort studies in order to increase participation in follow-up evaluations. We hypothesize that data collection through a mobile app will contribute to improvements in participation.

An accurate assessment of the potential benefits and drawbacks of using this mobile technology tool for data collection in cohort studies will be conducted. For such, the study will be conducted in three cohorts developed in different temporal, cultural, and geographic contexts, increasing the generalization of the results found. This evaluation is intended to contribute to the development of more appropriate tools for data collection and consequently to increase participation in epidemiological studies.

Conditions

  • Participants of Longitudinal Cohort Studies
  • Controls

Interventions

DEVICE

RECAP_MyLife mobile app

The intervention will be the use of a mobile application for collecting data from cohorts participants, envisioning to engage participants and collect continuous unbiased records. Participants in the intervention group will install the mobile application on their smartphones on the beginning of the trial and will be asked to self-report information on mood every day. Simultaneously, physical activity (number of steps) will be passively tracked through real-time information. Participants will complete baseline and post-intervention measures of mood status based on the "Circumplex Mood Model" and IPAQ-Short form. Following these measures, participants will be asked to complete questionnaires on usability (SUS scale) and acceptability of the intervention.

OTHER

Usual data collection methods

Participants in this group will provide data through usual types of data collection methods (face-to-face assessments, mailed questionnaires, online questionnaires).

Sponsors & Collaborators

  • Finnish Institute for Health and Welfare

    collaborator OTHER_GOV
  • Netherlands Organisation for Scientific Research

    collaborator OTHER_GOV
  • University of Tartu

    collaborator OTHER
  • Instituto de Saude Publica da Universidade do Porto

    lead OTHER

Principal Investigators

  • Henrique Barros, Professor · Institute of Public Health of the University of Porto (ISPUP)

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-02-28
Primary Completion
2021-04-30
Completion
2021-04-30

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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 NCT04714788 on ClinicalTrials.gov