Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:56 PM
Ignite Modification Date:
2025-12-24 @ 1:56 PM
NCT ID:
NCT04586595
Eligibility Criteria:
Inclusion Criteria:
* Participants who are able and willing to give written informed consent and are either:
* GPs in their final year of training who have received approval/permission from their GP trainer to participate in the study or;
* GP trainers with a trainee who has consented to take part in the pilot study or;
* Primary care pharmacists (employed by the practice, the primary care network (PCN) or the clinical commissioning group (CCG) in which the GP in training works) with ideally, at least 6-months experience of working in GP practices or;
* Pharmacists specially trained to deliver the REVISiT intervention and trained on good clinical practice (GCP) in research
Exclusion Criteria:
* Participants not able or willing to give written informed consent
* GP trainees with significant participation in other studies that could impact / could be impacted by their taking part in this randomised pilot study
* GP trainees who do not have the support of their trainer to participate in the study
* GP trainers who do not wish for their trainee to be involved with the study
* Pharmacists who do not have the required experience (ideally at least 6-month) of working in general practice in England
* Pharmacists who are not trained in delivering the REVISiT intervention or on GCP as part of this study
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT04586595
Study Brief:
Protocol Section:
NCT04586595