Last reviewed · How we verify
NCT03605381: MORe PREcISE
MORbidity PRevalence Estimate In StrokE
trial in Stroke in 500 participants. Status unknown.
31 August 2019
Quick facts
| Lead sponsor | Aneurin Bevan University Health Board |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 500 |
| Start date | 30 September 2018 |
| Primary completion | 31 August 2019 |
| Estimated completion | 30 September 2019 |
| Sites | 3 locations across United Kingdom |
Conditions studied
- Stroke — all drugs for Stroke →
- CVA (Cerebrovascular Accident) — all drugs for CVA (Cerebrovascular Accident) →
- CVA; Sequelae — all drugs for CVA; Sequelae →
- Stroke, Ischemic — all drugs for Stroke, Ischemic →
Sponsor
Aneurin Bevan University Health Board
Who can join
18 and older, any sex, with Stroke or CVA (Cerebrovascular Accident). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Information regarding the likely progress of post-stroke symptoms is vitally important to stroke survivors to allow them to plan for the future and to adjust to life after stroke. Moreover, the prevalence of morbidity secondary to stroke is of central importance to Health Professionals to understand the prognosis of the disease in the patients under their care. Additionally, it will also allow commissioners of care, planners and third sector organisations to adapt to and answer the needs of a post-stroke population. Currently, the data collected by national audit programmes are concentrated on what can be termed 'process or process of care' data. The utility of these data are in the ability to audit the care received by stroke survivors on stroke units against evidenced standards for care, thus ensuring evidence based practice. Nevertheless, process of care is only one form of measuring stroke unit care and the audit programmes collect some limited functional status data, data relating to risk-factor co-morbidities and treatment received data. Therefore, the scope of this study is to build on the minimum data set currently collected and to collect post-stroke data in domains not currently collected. The International Consortium for Health Outcomes Measurement (ICHOM) takes important steps to collect data outside of process of care data such as a Patient Reported outcome data in their minimum outcome data set for stroke \[currently under review\].. Nevertheless, the ICHOM doesn't currently advocate the specific collection of data relating to cognitive impairment or emotional problems secondary to stroke. It is in these important aspects that this study will augment the data set currently advocated by ICHOM to collect data in the areas of cognitive impairment and emotional problems secondary to stroke. Therefore, the aim of this study is to quantify the prevalence of morbidity at six months post-stroke.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Morbidity Prevalence Estimate at 6 Months Following a Stroke: Protocol for a Cohort Study.
Smith A, Bains N, Copeland L, Pennington A, et al · · 2020 · cited 2× · PMID 32512539 · DOI 10.2196/15851 -
E-Poster Viewing – Miscellaneous
· 2019
Verify or expand the search:
- PubMed search for NCT03605381
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Stroke
Currently open trials in the same condition.
- NCT06615973 — Screening for Social Determinants of Health (SDOH) and Cognitive Function in Individuals With History of Stroke · recruiting
- NCT07494890 — Measurement Properties of Mechanical Cost of Walking for Individuals With Walking Impairment · NA · recruiting
- NCT07356011 — Exoskeleton for Balance · NA · recruiting
- NCT07523503 — Unilateral Versus Bilateral Task-specific Training on Motor Impairment, Upper Extremity Function, and Hand Dexterity in · NA · recruiting
- NCT06704074 — Virtual Reality Task Oriented Training on Upper Limb Function in Stroke Patients · NA · recruiting
Other Aneurin Bevan University Health Board trials
Trials by the same sponsor.
- NCT04903756 — The PERCEIVE Study · completed
- NCT03692091 — Comparing Two Methods of Subacromial Space Injection · NA · unknown
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03605381 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Aneurin Bevan University Health Board
- Last refreshed: 5 July 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03605381.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing