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Headline
This study suggests that it is both acceptable and feasible to undertake a full sexual health promotion trial for people with serious mental health problems.
Abstract
Background:
People with serious mental illness have sexual health needs, but there is limited evidence regarding effective interventions to promote their sexual health.
Objectives:
To develop a sexual health promotion intervention for people with serious mental illness, and to conduct a feasibility trial in order to establish the acceptability and parameters for a fully powered trial.
Design:
A two-armed randomised controlled, open feasibility study comparing usual care alone with usual care plus the adjunctive intervention.
Setting:
Five community mental health providers in Leeds, Barnsley, Brighton and London.
Participants:
Adults aged ≥ 18 years with serious mental illness and receiving care from community mental health teams.
Interventions:
A remote, web-based computer randomisation system allocated participants to usual care plus the RESPECT (Randomised Evaluation of Sexual health Promotion Effectiveness informing Care and Treatment) intervention (three sessions of 1 hour) (intervention arm) or usual care only (control arm). The intervention was an interactive manualised package of exercises, quizzes and discussion topics focusing on knowledge, motivation and behavioural intentions to adopt safer sexual behaviours.
Main outcome measures:
Feasibility parameters including establishing the percentage of people who were eligible, consented and were retained in each arm of the trial, retention for the intervention, as well as the completeness of the data collection. Data were collected on knowledge, motivation to adopt safer sexual behaviour, sexual behaviour, sexual stigma, sexual health service use and quality of life. Data were collected at baseline and then at 3 months and 6 months post randomisation.
Results:
Of a target of 100 participants, 72 people participated in the trial over 12 months. Of the 36 participants randomised to the intervention arm, 27 received some of the intervention (75.0%). At 3 months, 59 of the 72 participants completed follow-up questionnaires (81.9%) (30 participants from the intervention arm and 29 participants from the control arm). Only the first 38 participants were followed up at 6 months. However, data were collected on 29 out of 38 participants (76.3% retention): 13 in the intervention arm and 16 in the control arm. No adverse events were reported. Participant feedback confirmed that both the design and the intervention were acceptable. The economic analysis indicated high completion rates and completeness of data among participants who continued the trial.
Conclusions:
Despite the limitations, the findings suggest that it is both acceptable and feasible to undertake a sexual health promotion study for people with serious mental illness.
Future work:
A fully powered randomised controlled trial would be required to establish the clinical effectiveness of the intervention.
Trial registration:
Current Controlled Trials ISRCTN15747739.
Funding:
This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 23, No. 65. See the NIHR Journals Library website for further project information.
Contents
- Plain English summary
- Scientific summary
- Chapter 1. Introduction and background
- Chapter 2. Stage 1: intervention development
- Background and theoretical basis
- Theoretical model: the information–motivation–behavioural skills model of health behaviour change
- Process of intervention development
- Session 1: knowledge of human immunodeficiency virus, sexually transmitted infections and safer sex
- Session 2: keeping safe – focus on the role of condoms and contraception choices
- Session 3: the RESPECT intervention – relationships and communication
- Chapter 3. Feasibility trial
- Trial design
- Sample size
- Approvals obtained
- Trial centres
- Patient and public involvement in the feasibility trial
- Recruitment
- Outcomes
- Secondary outcome assessment
- Randomisation
- Trial interventions
- Trial completion and exit
- Withdrawals
- Adverse events
- Statistical analysis
- Economic analysis methods
- Qualitative study
- Chapter 4. Protocol changes
- Chapter 5. Results
- Chapter 6. Feedback
- Chapter 7. Impact
- Chapter 8. Discussion and conclusions
- Acknowledgements
- References
- Appendix 1. Study summary
- Appendix 2. Additional statistical results tables
- List of abbreviations
- List of supplementary material
About the Series
Article history
The research reported in this issue of the journal was funded by the HTA programme as project number 14/172/01. The contractual start date was in February 2016. The draft report began editorial review in August 2018 and was accepted for publication in January 2019. The authors have been wholly responsible for all data collection, analysis and interpretation, and for writing up their work. The HTA editors and publisher have tried to ensure the accuracy of the authors’ report and would like to thank the reviewers for their constructive comments on the draft document. However, they do not accept liability for damages or losses arising from material published in this report.
Declared competing interests of authors
Catherine Hewitt reports being a member of the National Institute for Health Research Health Technology Assessment Commissioning Board.
Last reviewed: August 2018; Accepted: January 2019.
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