| scholarly article | Q13442814 |
| P50 | author | Til Wykes | Q7802018 |
| Jo Evans | Q58744971 | ||
| Angela Sweeney | Q58875780 | ||
| P2093 | author name string | Diana Rose | |
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| P433 | issue | 1 | |
| P921 | main subject | mental health | Q317309 |
| mental health services | Q67076049 | ||
| P304 | page(s) | 41-46 | |
| P577 | publication date | 2011-01-01 | |
| P1433 | published in | International Review of Psychiatry | Q15752216 |
| P1476 | title | A model for developing outcome measures from the perspectives of mental health service users | |
| P478 | volume | 23 |
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| Q45114474 | Contributions of people using mental health services as partners in teaching psychiatry |
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| Q57123903 | Developing a patient-reported experience questionnaire with and for people who use drugs: A community engagement process in Vancouver's Downtown Eastside |
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| Q97589032 | Development, reliability and validity of the case management quality of care scale (CMQS) among clients with first episode psychosis |
| Q37333340 | Expectations of new treatment in rheumatoid arthritis: developing a patient-generated questionnaire |
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| Q60631192 | Hacia una mayor incorporación de la perspectiva del paciente en el diseño de los instrumentos de evaluación de la efectividad y calidad de los cuidados |
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| Q90392540 | Individualized and Standardized Outcome Measures: Further Arguments in Favor of Cohabitation |
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| Q60206969 | Preliminary psychometric analyses of two assessment measures quantifying communicative and social activities: the COMACT and SOCACT |
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| Q34677417 | Service user- and carer-reported measures of involvement in mental health care planning: methodological quality and acceptability to users. |
| Q48177449 | Showing the Unsayable: Participatory Visual Approaches and the Constitution of 'Patient Experience' in Healthcare Quality Improvement |
| Q100567519 | The Recovering Quality of Life 10-item (ReQoL-10) scale in a first-episode psychosis population: Validation and implications for patient-reported outcome measures (PROMs) |
| Q86641619 | The contemporary state of service-user-led research |
| Q90087470 | The experience of mental health service users in health system strengthening: lessons from Uganda |
| Q52906285 | The impact of involvement on researchers: a learning experience. |
| Q55339459 | The importance of content and face validity in instrument development: lessons learnt from service users when developing the Recovering Quality of Life measure (ReQoL). |
| Q41962676 | The vicissitudes of the recovery construct; or, the challenge of taking "subjective experience" seriously |
| Q39134982 | To belong, contribute, and hope: first stage development of a measure of social recovery |
| Q50567198 | Towards a genuinely user-centred evaluation of harm reduction and drug treatment programmes: A further proposal. |
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| Q34298016 | Understanding service user-defined continuity of care and its relationship to health and social measures: a cross-sectional study |
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| Q93013041 | Using a person-generated mental health outcome measure in large clinical trials in Kenya and Pakistan: Self-perceived problem responses in diverse communities |
| Q33602378 | VOICE: developing a new measure of service users' perceptions of inpatient care, using a participatory methodology |
| Q47745528 | What side effects are problematic for patients prescribed antipsychotic medication? The Maudsley Side Effects (MSE) measure for antipsychotic medication |
| Q59768471 | “You’re all going to hate the word ‘recovery’ by the end of this”: Service users’ views of measuring addiction recovery |
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