Improving the heart health of individuals with abdominal aortic aneurysms: the CRISP Study

Conditions

Abdominal aortic aneurysm Circulatory System Abdominal aortic aneurysm, cardiovascular disease

Thomas M. Withers, Colin Greaves, Matthew J. Bown, Faye Ashton, Aimee J. Scott et al. (8 authors)

NIHR Open Research2024-09-03

10.3310/nihropenres.13596.2

A feasibility study of the CRISP intervention; a cardiovascular risk reduction intervention in patients with an abdominal aortic aneurysm

Thomas M. Withers, Colin Greaves, Matthew J. Bown, Faye Ashton, Aimee J. Scott et al. (8 authors)

NIHR Open Research2024-06-07

10.3310/nihropenres.13596.1

Improving cardiovascular health in patients with an abdominal aortic aneurysm: development of the cardiovascular risk reduction in patients with aneurysms (CRISP) behaviour change intervention.

Withers TM, Greaves CJ, Bown MJ, Saratzis A.

2024-01-293 citations

10.1186/s40814-024-01445-z

Interventions

There are two phases to this study, this registration concerns phase 2. In Phase 1, we will develop an intervention that will help patients with an abdominal aortic aneurysm improve their heart health

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: 1. Men with an abdominal aortic aneurysm identified through the existing NHS Abdominal Aortic Aneurysm (AAA) Screening Programme (NAAASP) 2. Any healthcare professional involved in the care of individuals with an abdominal aortic aneurysm

Exclusion criteria

Exclusion criteria: Age <18 years

Design outcomes

Primary

Measure	Time frame
1. Proportion of patients agreeing to take part out of all patients invited at six months (recruitment rate) measured using case report forms 2. Proportion of people recruited who provide data at the end of the intervention period i.e. at six months (retention rate) measured using case report forms 3. Percentage of intervention sessions that participants complete at six months (intervention uptake) measured using case report forms 4. Intervention acceptability to patients (assessed qualitatively using semi-structured interviews and a satisfaction questionnaire) and service providers (assessed qualitatively)	—

Measure

Time frame

1. Proportion of patients agreeing to take part out of all patients invited at six months (recruitment rate) measured using case report forms 2. Proportion of people recruited who provide data at the end of the intervention period i.e. at six months (retention rate) measured using case report forms 3. Percentage of intervention sessions that participants complete at six months (intervention uptake) measured using case report forms 4. Intervention acceptability to patients (assessed qualitatively using semi-structured interviews and a satisfaction questionnaire) and service providers (assessed qualitatively)

—

Secondary

Measure	Time frame
There are no secondary outcome measures	—

Countries

England, United Kingdom

Contacts

Public ContactAnn Elsworth

ame29@le.ac.uk+44 (0)116 2502381

Outcome results

None listed