Psychosocial Intervention Using Online Resources to Promote Personal Recovery in Users of Specialist Mental Health Services
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Schizophrenia
- Sponsor
- Swinburne University of Technology
- Enrollment
- 148
- Locations
- 10
- Primary Endpoint
- Change in Process of Recovery Questionnaire (QPR)
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
This project is a component of a broader research program referred to as "Self-Management and Recovery Technology (SMART): Use of online technology to promote self-management and recovery in people with psychosis", which has been funded by the Victorian Department of Health Mental Illness Research Fund (MIRF33). The overall research program is examining the therapeutic potential of using online (Internet-based) educational and multimedia resources in mental health services. It involves the development of a website which can be accessed via an internet browser on a desktop computer, tablet computer, or smartphone. It consists of a series of educational modules containing textual information, exercises, audio, and video clips designed to promote self-management and recovery in people with a history of persisting mental illness.
This particular project (SMART-Therapy) involves a randomised controlled trial examining the use of a discrete 8-session psychosocial intervention delivered in addition to routine care which utilises these online materials. The intervention will involve a mental health worker meeting with the participant with a tablet computer (e.g. iPad) on which online materials can be viewed, and used to guide an interaction with the participant.
The randomised controlled trial will include 148 participants, who will be randomised to receive one of two interventions: (a) meeting with a support worker using the SMART website to guide interaction (health intervention), or (b) meeting with a support worker delivering a social interaction-based control condition (social intervention). In each condition, there will be 8 x 50min face-to-face sessions over 3 months. Assessments will be completed pre-randomisation, and at 3, 6 and 9 months.
The primary hypothesis is that participants randomised to the health intervention will show greater improvement in personal recovery than participants randomised to the social intervention, and that these improvements will be maintained at follow-up (6 and 9 months following intake).
Investigators
Eligibility Criteria
Inclusion Criteria
- •diagnosis of a functional psychotic disorder (schizophrenia-related disorder OR bipolar disorder or major depressive disorder with the presence of a severe episode with psychotic features within the past 2 years);
- •sufficient fluency in English to make use of the resources;
- •overall intellectual functioning within normal limits (WTAR estimated IQ\>70);
- •Exclusion criteria (e) change in medication or in-patient admission in the previous 2 months;
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Change in Process of Recovery Questionnaire (QPR)
Time Frame: Baseline, 3, 6 and 9 months
Assesses personal recovery
Secondary Outcomes
- Change in Positive and Negative Syndrome Scales (PANSS)(Baseline, 3, 6 and 9 months)
- Change in Assessment of Quality of Life 8dimension (AQol8d)(Baseline, 3, 6 and 9 months)
- Change in Resource Use Questionnaire(Baseline, 3, 6 and 9 months)
- Change in Depression Anxiety Stress Scale (DASS-21)(Baseline, 3, 6 and 9 months)
- Change in Subjective Experience of Psychosis Scale (SEPS)(Baseline, 3, 6 and 9 months)