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Reducing cognitive decline and dementia by lowering blood pressure pilot I study

RECALL – REducing Cognitive decline and dementiA by Lowering bLood pressure - Pilot I

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
ISRCTN
Registry ID
ISRCTN43958304
Enrollment
110
Registered
2019-10-07
Start date
2019-11-01
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive decline Mental and Behavioural Disorders Cognitive decline

Interventions

Potential participants will be invited to visit a study web page by letter of invitation. On this study webpage they can read the participant information documentation and then complete an electronic

Sponsors

University of Dundee/NHS Tayside
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Over 60 years old 2. Valid email address (per participant) 3. Able to access the internet

Exclusion criteria

Exclusion criteria: 1. GPs may exclude participants who they deem unsuitable to participate 2. Clinical diagnosis of dementia, treatment with medication for dementia or cognitively unable to follow the protocol (investigator opinion)

Design outcomes

Primary

MeasureTime frame
1. Recruitment numbers 2. Protocol adherence Timepoint: End of pilot

Secondary

MeasureTime frame
1. Assess suitability of online cognitive testing for study cohort Outcome measures: Proportion of participants who complete a baseline test 2. Assess baseline cognitive function Outcomes measures: Proportion of study population completing online screening cognitive function test, and scores obtained 3. Assess feasibility of requiring each participant to identify two individuals who agree to act as alternative contacts Outcome measures: Proportion of participants who have two consenting alternative contacts 4. Assess feasibility of home blood pressure monitoring using study supplied HBPM machine Outcome measures: Proportion of participants submitting a complete set of home BP measurements 5. Assess baseline blood pressure suitability of study cohort Outcome measures: Proportion of participants with a home BP submission averaging 140mmHg or below systolic 6. Assess feasibility of using portable i-STAT Alinity device for providing blood results Outcome measures: Proportion of blood results obtained using portable system 7. Assess the likely number of eligible patients signing up Outcome measures: Proportion of those invited who meet proposed formal study entry criteria

Countries

Scotland, United Kingdom

Contacts

Public ContactEvelien Rooke
e.rooke@dundee.ac.uk+44 (0) 1382 383119

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jun 11, 2026