ISRCTN16488358已完成未知
Enhancing the quality of user involved care planning in mental health services (EQUIP): clinical randomised controlled trial and process evaluation - cluster cohort randomised controlled trial
Manchester Mental Health & Social Care Trust (UK)0 个研究点目标入组 480 人开始时间: 2014年5月14日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 480
研究概览
简要总结
- 2015 protocol in http://www.ncbi.nlm.nih.gov/pubmed/26268221 2. 2016 results in https://www.ncbi.nlm.nih.gov/pubmed/26963252 3. 2015 results in https://www.ncbi.nlm.nih.gov/pubmed/26243762 4. 2015 results in https://www.ncbi.nlm.nih.gov/pubmed/26253574 5. 2015 results in https://www.ncbi.nlm.nih.gov/pubmed/26268221 6. 2017 results in https://www.ncbi.nlm.nih.gov/pubmed/29144591 7. 2016 results in https://www.ncbi.nlm.nih.gov/pubmed/27931210 8. 2015 results in https://www.ncbi.nlm.nih.gov/pubmed/26519298 9. 2015 results in https://www.ncbi.nlm.nih.gov/pubmed/26319602 10. 2017 results in https://www.ncbi.nlm.nih.gov/pubmed/28105690 11. 2014 results in https://www.ncbi.nlm.nih.gov/pubmed/25566099 12. 2017 results in https://www.ncbi.nlm.nih.gov/pubmed/28218977 13. 2015 results in https://www.ncbi.nlm.nih.gov/pubmed/26634415 14. 2016 results in https://www.ncbi.nlm.nih.gov/pubmed/27931252
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Current inclusion criteria as of 01/06/2015:
- •All community mental health teams (and health professionals therein) within the 10 mental health trust locations will be eligible for inclusion.
- •Service users aged 18 and over with a severe mental illness (e.g., psychosis, manic depressive illness) under the care of participating community mental health teams will be eligible for inclusion for both the cluster cohort sample and cluster cross sectional sample. However, those who participate in the cluster cohort sample will not be eligible to also take part in the cluster cross sectional sample.
- •Service users will be asked at the point of consent to identify a carer that might be willing to be included in the study. All carers over the age of 18 will be eligible for inclusion in the cluster cohort study. All service users and carers who consent to the cluster cohort study will be eligible to take part in the process evaluation. All professionals in the relevant community mental health teams will be eligible to take part in the process evaluation.
- •Previous inclusion criteria:
- •All community teams and rehabilitation inpatient facilities (and health professionals therein) within the Manchester and Nottingham locations will be eligible for inclusion.
- •Service users aged 18 and over with a severe mental illness (e.g., psychosis, manic depressive illness) under the care of participating community teams and rehabilitation inpatient facilities will be eligible for inclusion for both the cluster cohort sample and cluster cross sectional sample. However, those who participate in the cluster cohort sample will not be eligible to also take part in the cluster cross sectional sample.
- •Service users will be asked at the point of consent to identify a carer that might be willing to be included in the study. All carers over the age of 18 will be eligible for inclusion in the cluster cohort study. All service users and carers who consent to the cluster cohort study will be eligible to take part in the process evaluation. All professionals in the relevant community teams and rehabilitation inpatient facilities will be eligible to take part in the process evaluation.
排除标准
- •Current exclusion criteria as of 01/06/2015:
- •Service users will be excluded if their participation is judged as inappropriate by clinical staff within the relevant community mental health teams . The principal exclusion criteria will be an inability to provide informed consent. We will seek to document all exclusions and report them as part of the trial CONSORT diagram.
- •Previous exclusion criteria:
- •Service users will be excluded if their participation is judged as inappropriate by clinical staff within the relevant community teams and rehabilitation inpatient facilities. The principal exclusion criteria will be an inability to provide informed consent. We will seek to document all exclusions and report them as part of the trial CONSORT diagram.
研究者
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