We use cookies to help provide you with the best possible online experience.
By using this site, you agree that we may store and access cookies on your device. Cookie policy.
Cookie settings.
Functional Cookies
Functional Cookies are enabled by default at all times so that we can save your preferences for cookie settings and ensure site works and delivers best experience.
3rd Party Cookies
This website uses Google Analytics to collect anonymous information such as the number of visitors to the site, and the most popular pages.
Keeping this cookie enabled helps us to improve our website.
PROMDEP
Patient-reported outcome measures for monitoring primary care patients with depression – randomised controlled trial.
The PROMDEP RCT will look at whether giving personal feedback to people being treated for depression might help them get better more quickly. This will be done by using the PHQ-9 depression symptom questionnaire as a patient reported outcome measure (or 'PROM') and feeding back the results to the patients themselves, and the practitioners looking after them, together with brief suggestions for treatment relevant to the severity of the patient’s depression.
The aim is to answer the following research question: What is the effectiveness and cost-effectiveness of assessing primary care patients with depression or low mood soon after diagnosis and again at follow-up 10-35 days later, using the PHQ-9 questionnaire combined with patient and practitioner feedback and guidance on treatment?
This is a cluster randomised controlled trial so whole practices will be randomly allocated to either:
- Intervention arm, where patients will complete the PHQ-9, to inform treatment.
- Control arm, where participants will receive usual treatment, but will not use the PHQ-9.
Who can take part?
Who can take part?
- Patients presenting with a new episode of depression
- 18+ years of age
- Sufficiently fluent in English to participate
This study is now closed
- Thanks to any patients at Bay Medical Group who have taken part