Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trial
Objectives To test the feasibility and acceptability of a randomised controlled trial (RCT) to evaluate a Smartphone-based self-management tool in Early Intervention in Psychosis (EIP) services.Design A two-arm unblinded feasibility RCT.Setting Six NHS EIP services in England.Participants Adults usi...
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
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BMJ Publishing Group
2020-08-01
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| Series: | BMJ Open |
| Online Access: | https://bmjopen.bmj.com/content/10/8/e034927.full |
| _version_ | 1818727770954399744 |
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| author | Rebecca Jones Thomas Steare Puffin O’Hanlon Michelle Eskinazi David Osborn Brynmor Lloyd-Evans Helen Rostill Sarah Amani Sonia Johnson |
| author_facet | Rebecca Jones Thomas Steare Puffin O’Hanlon Michelle Eskinazi David Osborn Brynmor Lloyd-Evans Helen Rostill Sarah Amani Sonia Johnson |
| author_sort | Rebecca Jones |
| collection | DOAJ |
| description | Objectives To test the feasibility and acceptability of a randomised controlled trial (RCT) to evaluate a Smartphone-based self-management tool in Early Intervention in Psychosis (EIP) services.Design A two-arm unblinded feasibility RCT.Setting Six NHS EIP services in England.Participants Adults using EIP services who own an Android Smartphone. Participants were recruited until the recruitment target was met (n=40).Interventions Participants were randomised with a 1:1 allocation to one of two conditions: (1) treatment as usual from EIP services (TAU) or (2) TAU plus access to My Journey 3 on their own Smartphone. My Journey 3 features a range of self-management components including access to digital recovery and relapse prevention plans, medication tracking and symptom monitoring. My Journey 3 use was at the users’ discretion and was supported by EIP service clinicians. Participants had access for a median of 38.1 weeks.Primary and secondary outcome measures Feasibility outcomes included recruitment, follow-up rates and intervention engagement. Participant data on mental health outcomes were collected from clinical records and from research assessments at baseline, 4 months and 12 months.Results 83% and 75% of participants were retained in the trial at the 4-month and 12-month assessments. All treatment group participants had access to My Journey 3 during the trial, but technical difficulties caused delays in ensuring timely access to the intervention. The median number of My Journey 3 uses was 16.5 (IQR 8.5 to 23) and median total minutes spent using My Journey 3 was 26.8 (IQR 18.3 to 57.3). No serious adverse events were reported.Conclusions Recruitment and retention were feasible. Within a trial context, My Journey 3 could be successfully delivered to adults using EIP services, but with relatively low usage rates. Further evaluation of the intervention in a larger trial may be warranted, but should include attention to implementation.Trial registration ISRCTN10004994. |
| first_indexed | 2024-12-17T22:19:23Z |
| format | Article |
| id | doaj.art-a959a5b5778c430e8d021242d6901860 |
| institution | Directory Open Access Journal |
| issn | 2044-6055 |
| language | English |
| last_indexed | 2024-12-17T22:19:23Z |
| publishDate | 2020-08-01 |
| publisher | BMJ Publishing Group |
| record_format | Article |
| series | BMJ Open |
| spelling | doaj.art-a959a5b5778c430e8d021242d69018602022-12-21T21:30:31ZengBMJ Publishing GroupBMJ Open2044-60552020-08-0110810.1136/bmjopen-2019-034927Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trialRebecca Jones0Thomas Steare1Puffin O’Hanlon2Michelle Eskinazi3David Osborn4Brynmor Lloyd-Evans5Helen Rostill6Sarah Amani7Sonia Johnson8Division of Psychiatry, University College London, London, UKDivision of Psychiatry, University College London, London, UKDivision of Psychiatry, University College London, London, UKDivision of Psychiatry, University College London, London, UKDivision of Psychiatry, UCL, London, UKDivision of Psychiatry, University College London, London, UKUniversity of Surrey, Guildford, Surrey, UKEarly Intervention in Psychosis Programme (South of England), Oxford, UKDivision of Psychiatry, University College London, London, UKObjectives To test the feasibility and acceptability of a randomised controlled trial (RCT) to evaluate a Smartphone-based self-management tool in Early Intervention in Psychosis (EIP) services.Design A two-arm unblinded feasibility RCT.Setting Six NHS EIP services in England.Participants Adults using EIP services who own an Android Smartphone. Participants were recruited until the recruitment target was met (n=40).Interventions Participants were randomised with a 1:1 allocation to one of two conditions: (1) treatment as usual from EIP services (TAU) or (2) TAU plus access to My Journey 3 on their own Smartphone. My Journey 3 features a range of self-management components including access to digital recovery and relapse prevention plans, medication tracking and symptom monitoring. My Journey 3 use was at the users’ discretion and was supported by EIP service clinicians. Participants had access for a median of 38.1 weeks.Primary and secondary outcome measures Feasibility outcomes included recruitment, follow-up rates and intervention engagement. Participant data on mental health outcomes were collected from clinical records and from research assessments at baseline, 4 months and 12 months.Results 83% and 75% of participants were retained in the trial at the 4-month and 12-month assessments. All treatment group participants had access to My Journey 3 during the trial, but technical difficulties caused delays in ensuring timely access to the intervention. The median number of My Journey 3 uses was 16.5 (IQR 8.5 to 23) and median total minutes spent using My Journey 3 was 26.8 (IQR 18.3 to 57.3). No serious adverse events were reported.Conclusions Recruitment and retention were feasible. Within a trial context, My Journey 3 could be successfully delivered to adults using EIP services, but with relatively low usage rates. Further evaluation of the intervention in a larger trial may be warranted, but should include attention to implementation.Trial registration ISRCTN10004994.https://bmjopen.bmj.com/content/10/8/e034927.full |
| spellingShingle | Rebecca Jones Thomas Steare Puffin O’Hanlon Michelle Eskinazi David Osborn Brynmor Lloyd-Evans Helen Rostill Sarah Amani Sonia Johnson Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trial BMJ Open |
| title | Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trial |
| title_full | Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trial |
| title_fullStr | Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trial |
| title_full_unstemmed | Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trial |
| title_short | Smartphone-delivered self-management for first-episode psychosis: the ARIES feasibility randomised controlled trial |
| title_sort | smartphone delivered self management for first episode psychosis the aries feasibility randomised controlled trial |
| url | https://bmjopen.bmj.com/content/10/8/e034927.full |
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