A Mobile App to Improve Participation in Following-up Cohorts
NCT04714788 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 310
Last updated 2021-01-19
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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