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Clinical Trials/NCT00866099
NCT00866099
Unknown
Phase 2

Evidence-based Interventions In Dementia EVIDEM-ED: Early Recognition and Response in Primary Care

University College, London2 sites in 1 country125 target enrollmentJuly 2009
ConditionsDementia

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Dementia
Sponsor
University College, London
Enrollment
125
Locations
2
Primary Endpoint
An increase in the proportion of patients with dementia receiving two dementia reviews per year, from 20% to 50%
Last Updated
16 years ago

Overview

Brief Summary

The purpose of this study is to develop and test an educational intervention for dementia in primary care, combining timely diagnosis, psychosocial support around the period of diagnosis and management concordant with guidelines.

Detailed Description

Dementia presents many challenges for primary care. Early diagnosis is important as this allows those with dementia and their family care networks to engage with support services and plan for the future. These actions can relieve the significant psychological distress that people with dementia and close supporters may experience , and provide knowledge about the availability of medical and psycho-social support that can improved functioning and morale The main efforts to improve the identification and diagnosis of dementia should logically be targeted at primary care as this is the first point of contact for most individuals and their carers when faced with experiences of 'ill health'. There is, however, evidence that dementia remains under-detected and sub-optimally managed in general practice . An educational intervention that could enhance clinical practice, improving the skills of practitioners in the recognition of and response to dementia syndromes, could therefore be beneficial to people with dementia and their families, and potentially to health and social services.

Registry
clinicaltrials.gov
Start Date
July 2009
End Date
September 2012
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients with memory or other cognitive impairments suggestive of dementia syndrome
  • those with a formal diagnosis of dementia, of any type.

Exclusion Criteria

  • Patients and carers who are already involved in concurrent research
  • If the key professional feels that an approach to the person with dementia or their carer would be inappropriate, for example the dementia is very severe, or that an approach may increase distress
  • and any other important reason that the key professional may have for why the person with dementia or their carer should not be contacted.

Outcomes

Primary Outcomes

An increase in the proportion of patients with dementia receiving two dementia reviews per year, from 20% to 50%

Time Frame: twelve month follow up

Secondary Outcomes

  • quality of life, met and unmet need in carers and/or people with dementia(twelve month follow up)
  • documented concordance with intervention recommendations on recording disclosure decisions & consequences(twelve month follow up)
  • documented concordance with screening for depression(twelve month follow up)
  • documented concordance with referral to social services(twelve month follow up)
  • documented concordance with informing people with dementia and their carers about relevant local voluntary organisations(twelve month follow up)
  • documented concordance with provision of legal information(twelve month follow up)
  • documented concordance with shared management of cholinesterase inhibitor medication(twelve month follow up)

Study Sites (2)

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