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A Mobile Phone Self-Monitoring Tool to Increase Emotional Self-Awareness and Reduce Depression in Young People

Not Applicable
Completed
Conditions
Depression
Interventions
Device: Mobile Tracking Young People's Experiences (mobiletype)
Registration Number
NCT00794222
Lead Sponsor
Murdoch Childrens Research Institute
Brief Summary

The mobiletype program is a mental health assessment and monitoring tool that runs on mobile phones.

The program assesses the general mental health of young people in real-time and transmits this data to a website to be reviewed by their general practitioner (GP) in consultation with their patient. The website consists of individualised feedback reports for each participant, and graphical displays of the monitoring data. The primary aims of the current project are to examine: (1) whether the process of self-monitoring via the mobiletype program increases young people's awareness of their mood and reduces depressive symptoms and (2) whether emotional self-awareness mediates the relationship between self-monitoring and depressive symptoms.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
118
Inclusion Criteria
  • Aged 14 - 24 years of age
  • Proficient English
  • Patients must be deemed to have an emotional/mental health concern by their GP or be screened to have at least a mild mental health problem (a score of 16 or above) on the K10 Symptom Scale
Exclusion Criteria
  • Severe psychiatric or medical condition that prevents the person from complying with either the requirements of informed consent or the study protocol.
  • Young people referred to a mental health specialist by their GP will be excluded only if they obtain a specialist appointment during the mobiletype study period (2 - 4 weeks).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Mood monitoringMobile Tracking Young People's Experiences (mobiletype)The mobiletype monitoring intervention group will monitor their current activities, current mood, responses to negative mood, any recent stressors and coping strategies. Other activities monitored include eating patterns, exercise patterns, quantity and quality of sleep and alcohol and cannabis use.
Primary Outcome Measures
NameTimeMethod
Depressive symptomsPre-, post-monitoring, 6-week follow up & 6 month follow-up
Emotional Self AwarenessPre-, post-, 6-weeks post- and 6-months post-test
Secondary Outcome Measures
NameTimeMethod
Detection of mental health problemsPre-, post-monitoring, 6 week and 6 month follow up
Pathways to carePre-, post-monitoring, 6 week and 6 month follow up
Patient's satisfaction with their GPPre-, post-monitoring, 6 week and 6 month follow up

Trial Locations

Locations (1)

Clifton Hill Medical Centre

🇦🇺

Melbourne, Victoria, Australia

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