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Self-Management and Recovery Technology Psychosocial Intervention Trial

Psychosocial Intervention Using Online Resources to Promote Personal Recovery in Users of Specialist Mental Health Services

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02474524
Acronym
SMARTTherapy
Enrollment
148
Registered
2015-06-17
Start date
2015-01-01
Completion date
2017-07-31
Last updated
2017-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Affective Disorders, Psychotic, Psychotic Disorders, Schizophrenia

Keywords

Psychosis, Schizophrenia, Self-management, Recovery, Tablet computer, Digital health, Internet, Online, Peer support

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).

Interventions

Participants will receive 8 50-minute sessions during a 3 month window with a mental health worker, in addition to their routine care. Sessions will be structured by the worker and participant using a tablet computer to view materials on mental health self-management and personal recovery on a dedicated website for the trial. These will include information, videos, audio and exercises. Online materials make particular use of videos featuring people with lived experience of psychosis discussing how they have dealt with issues in their recovery, and will allow users to post comments on videos and in a forum. Participants may access online materials both during intervention sessions and outside sessions using any Internet-enabled device.

Participants will receive 8 50-minute sessions during a 3 month window with a mental health worker in addition to routine care (treatment as usual). The social intervention will utilise a computer tablet (i.e., iPad) servicing online resources to extend a manualised befriending intervention, based upon social interaction, designed to control for therapist contact and computer use. Each session will involve interaction about non-health related topics of interest to the participants, which will be facilitated by use of viewing online material related to these interests on a tablet computer as a prompt to conversation.

Sponsors

The Alfred
CollaboratorOTHER
St Vincent's Hospital Melbourne
CollaboratorOTHER
Melbourne Health
CollaboratorOTHER
Mental Illness Fellowship of Victoria
CollaboratorUNKNOWN
Mind Australia
CollaboratorOTHER
La Trobe University
CollaboratorOTHER
Deakin University
CollaboratorOTHER
Austin Health
CollaboratorOTHER_GOV
Neami National
CollaboratorUNKNOWN
Peninsula Health
CollaboratorOTHER_GOV
Eastern Health
CollaboratorOTHER
EACH
CollaboratorUNKNOWN
Swinburne University of Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. 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); 2. sufficient fluency in English to make use of the resources; 3. 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;

Design outcomes

Primary

MeasureTime frameDescription
Change in Process of Recovery Questionnaire (QPR)Baseline, 3, 6 and 9 monthsAssesses personal recovery

Secondary

MeasureTime frameDescription
Change in Positive and Negative Syndrome Scales (PANSS)Baseline, 3, 6 and 9 monthsAssesses psychotic symptomatology
Change in Subjective Experience of Psychosis Scale (SEPS)Baseline, 3, 6 and 9 monthsAssesses subjective impact of psychotic symptoms
Change in Depression Anxiety Stress Scale (DASS-21)Baseline, 3, 6 and 9 monthsAssesses emotional symptoms
Change in Assessment of Quality of Life 8dimension (AQol8d)Baseline, 3, 6 and 9 monthsAssesses quality of life
Change in Resource Use QuestionnaireBaseline, 3, 6 and 9 monthsMeasure of health service use

Other

MeasureTime frame
Change in General Self-Efficacy ScaleBaseline, 3, 6 and 9 months
Change in Schizophrenia Hope ScaleBaseline, 3, 6 and 9 months
Change in UCLA Loneliness ScaleBaseline, 3, 6 and 9 months
Change in Internalised Stigma of Mental Illness ScaleBaseline, 3, 6 and 9 months
Change in Self-Efficacy for Personal Recovery ScaleBaseline, 3, 6 and 9 months

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026