Trial · NCT07894354
Pilot Study to Co-create and Implement a Multicomponent Intervention to Reduce Mental Health Stigma in Primary Care
NCT07894354, Not applicable, Not yet recruiting, Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Pilot Study to Co-create and Implement a Multicomponent Intervention to Reduce Mental Health Stigma in Primary Care. Trials, record NCT07894354. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07894354
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Pilot Study to Co-create and Implement a Multicomponent Intervention to Reduce Mental Health Stigma in Primary Care
- NCT number
- NCT07894354
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 60 participants, estimated
- Lead sponsor
- Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
- Conditions
- Mental Health, Stigma of Mental Illness
- Interventions
- Multicomponent anti-stigma educational intervention for primary care professionals
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Professional recruitment rate (Feasibility) | At completion of recruitment at each participating center, up to 6 months after recruitment initiation | Proportion of eligible primary care professionals who enroll in the study among those invited to participate. The outcome will be reported as a percentage. |
| Primary | Intervention completion rate (Feasibility) | At completion of recruitment at each participating center, up to 6 months after recruitment initiation | Proportion of enrolled participants who complete the planned ODISSEA educational intervention. Completion will be defined as completion of the required intervention components according to the final intervention format established before implementation. The outcome will be reported as a percentage. |
| Primary | Completeness of outcome data (Feasibility) | Baseline (T0) through immediately after completion of the intervention (T1) | Proportion of enrolled participants with complete baseline (T0) and immediate post-intervention (T1) study assessments. The outcome will be reported as the percentage of participants with complete paired assessments. |
| Primary | Acceptability and satisfaction assessed with the Client Satisfaction Questionnaire (CSQ-8) | Immediately after completion of the intervention (T1) | Acceptability and satisfaction will be assessed after the intervention using the Client Satisfaction Questionnaire (CSQ-8). The instrument contains 8 items with 4 response options and yields a total score ranging from 8 to 32, with higher scores indicating greater satisfaction with the intervention. |
| Secondary | Change in mental health stigma-related attitudes measured with the OMS-HC-15 | Baseline (T0) and immediately after completion of the intervention (T1) | Stigma-related attitudes among primary care professionals will be assessed using the 15-item Opening Minds Stigma Scale for Health Care Providers (OMS-HC-15), with 5-point Likert response options. The same scale will be administered before and immediately after the intervention to estimate within-participant pre-post change. |
| Secondary | Change in knowledge about mental health stigma and related primary care practices | Baseline (T0) and immediately after completion of the intervention (T1) | Knowledge will be assessed using a brief study-specific questionnaire with true/false/don't know items covering recovery, risk, respectful language, autonomy and rights, administrative interactions, and diagnostic overshadowing. The same questionnaire will be administered at T0 and T1. Items will be analyzed individually and, if prespecified in the statistical analysis plan, may also be summarized as an overall knowledge score. |
| Secondary | Change in intention to modify professional practice | Baseline (T0) and immediately after completion of the intervention (T1) | Intention to change professional practice will be assessed using a study-specific 5-item questionnaire with 4-point Likert response options. Items address intended changes in communication, use of stigmatizing labels or expressions, diagnostic reasoning, patient participation in decision-making, and team processes. The same items and response scale will be administered at T0 and T1. |
| Other | Perceived applicability of the intervention to routine primary care practice | Immediately after completion of the intervention (T1) | Perceived applicability of the ODISSEA intervention to routine primary care practice will be assessed immediately after the intervention using a study-specific 5-point Likert item. Higher scores will indicate greater perceived applicability. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07894354
GET https://conductscience.org/api/trials/v1/NCT07894354/registered