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Improving Identification of Familial Hypercholesterolaemia in Primary Care (FAMCAT)

Not Applicable
Conditions
Familial Hypercholesterolemia
Interventions
Other: FAMCAT
Registration Number
NCT03934320
Lead Sponsor
University of Nottingham
Brief Summary

Multi-centre, non-randomised, non-controlled quasi-experimental study with nested qualitative study and economic appraisal.

Improving the identification of patients at high risk of cardiovascular disease in primary care, caused by conditions such as familial hypercholesterolaemia (FH), is a well-recognised national priority to prevent morbidity and mortality by early effective intervention.

This study will prospectively evaluate the clinical utility of the new primary care FH identification tool (FAMCAT) for identifying undiagnosed FH in routine primary care practice; and to assess its appropriateness, acceptability and cost-effectiveness.

This study will answer the following research questions (RQ):

1. What is the detection rate for new genetically-confirmed FH cases using the FAMCAT algorithm?

2. Is the FAMCAT tool appropriate and acceptable to practitioners and patients?

3. How can the FAMCAT tool be optimised to improve identification of FH?

4. What is the potential cost-effectiveness of the FAMCAT tool compared with current practice to identify patients with FH?

5. Can the FAMCAT intervention be improved?

6. What definitive study design and outcome measures are needed to provide robust evidence on whether to introduce FAMCAT into primary care practice?

RQ(1) \& (3) will be answered by a quasi-experimental diagnostic accuracy study; RQ(2) \& (5) answered by qualitative study; RQ (4) answered by economic appraisal and RQ(6) informed by all previous studies.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
400
Inclusion Criteria

Patients - General practices

  • Able to give written informed consent
  • 18 years of age or over
  • Serum cholesterol recorded in General Practice (GP) electronic records
  • Registered with a participating GP practice
  • Able to complete the self-administered questionnaires in English
  • No previous recorded diagnosis of familial hypercholesterolaemia in their GP electronic health records
  • Considered by their General Practitioner(s) to be appropriate to recruit to the study.

Patients - Secondary care

  • Able to give written informed consent
  • 18 years of age or over
  • Referred to or under the care of participating Trusts (e.g. lipid clinics)
  • Able to understand the study information and consent in English
  • Considered by their healthcare professions to be appropriate to recruit to the study.

Staff

  • Able to give written informed consent
  • 18 years of age or over
  • Working at a participating General Practice, Clinical Commissioning Group (CCG) or Secondary Care Trust.

Nominal Group

  • Able to give written informed consent
  • 18 years of age or over
  • A FH stakeholder (including specialists, primary care commissioners, FH patient representative)
Exclusion Criteria

Patients - General practices

  • Unable to give written informed consent
  • Under 18 years of age
  • Serum cholesterol not recorded in GP electronic records
  • Not registered with a participating GP practice
  • Unable to complete the self-administered questionnaires in English
  • Has a diagnosis of familial hypercholesterolaemia in their GP electronic records
  • Unable to have a blood test (for medical or personal reasons)
  • Have an opt-out code where patients has declined electronic medical records examined
  • Considered by their General Practitioner(s) to be inappropriate to recruit due to psycho-social reasons, participating in another related clinical trial or significant health reasons, e.g. terminal illness/diagnosis.

Patients - Secondary care

  • Unable to give written informed consent
  • Under 18 years of age
  • Not referred to or under the care of participating Trusts (e.g. lipid clinics)
  • Unable to understand the study information and consent in English
  • Considered by their healthcare professionals to be inappropriate to recruit to the study.

Staff

  • Unable to give written informed consent
  • Under 18 years of age
  • Has not worked at a participating General Practice, CCG or Secondary Care Trust.

Nominal Group

  • Unable to give written informed consent
  • Under 18 years of age
  • Not an FH stakeholder or FH patient representative

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
FAMCATFAMCAT-
Primary Outcome Measures
NameTimeMethod
Detection of genetically confirmed new FH cases using case identification tool (FAMCAT)Through study completion, an average of 2 years

Efficacy measure: Proportion (%) of genetically-confirmed FH cases Proportion (%) of genetically-confirmed FH cases

Secondary Outcome Measures
NameTimeMethod
Acceptability of FAMCATThrough study completion, an average of 2 years.

Efficacy measure: representativeness of qualitative interview sample. Key themes will be identified from qualitative interview transcripts of patient experience of participating in the study, acceptability of the study procedures (ie. location of blood test clinic appointments, waiting time to receive test results) , and appropriateness of methods of contact with study participants (ie. format and content of study materials, communicating test results). Key themes on usability will be identified from qualitative interview transcripts of health care professionals who used the FAMCAT tool clinically (ie. search criteria for clinical records, interpretation of results)

Usability of FAMCATThrough study completion, an average of 2 years.

Efficacy measure: representativeness of qualitative interview sample. Key themes on usability will be identified from qualitative interview transcripts of health care professionals who used the FAMCAT tool clinically (ie. search criteria for clinical records, interpretation of results)

Appropriateness of FAMCATThrough study completion, an average of 2 years.

Efficacy measure: representativeness of qualitative interview sample. Key themes will be identified from qualitative interview transcripts of patient experience of appropriateness of methods of contact with study participants (ie. format and content of study materials, communicating test results).

Self-reported anxiety measures for use in a future trialBaseline to 15 months after genetic test results reported

Anxiety measured using 6 item Spielberger State-Trait Anxiety Inventory (STAI). The total score will be calculated at study entry, after receiving genetic test results and 12- 15 months after genetic tests results received

Beliefs about predisposition to coronary heart diseaseBaseline to 15 months after genetic test results reported

Beliefs on causes for heart disease were assessed using 8 items, from a total of 18 items, which comprise the 'Causes of my illness' subscale in the Revised Illness Perception Questionnaire, IPQ-R.

The distribution of data for each one of the 8 questions will be presented at study entry, after receiving genetic test results and 12- 15 months after genetic tests results received

Self-reported lifestyle change measures for use in a future trialBaseline to 15 months after genetic test results reported

Stages of change for smoking cessation and physical activity will be measured. The five stages of change will be dichotomised into: (1) pre-contemplation, contemplation and preparation and (2) action/maintenance. The distribution of proportions for each measure will be presented at study entry, after receiving genetic test results and 12- 15 months after genetic tests results received

Cost-effective FAMCAT threshold to identify genetically confirmed FHthrough study completion, an average of 2 years

Efficacy measure: Primary analysis:

Incremental cost-effectiveness ratio (ICER) of FAMCAT compared to Simon-Broome criteria; Sensitivity analysis: Incremental costeffectiveness ratio (ICER) of FAMCAT at different testing thresholds. Short-term model: 24 Months

Trial Locations

Locations (1)

Division of Primary Care, University of Nottingham

🇬🇧

Nottingham, Nottinghamshire, United Kingdom

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