TAHOC: The Impact of Dementia and Neurocognitive Disorders on Hypertension Treatment in the Elderly

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Completed
CT.gov ID
NCT05845736
Collaborator
(none)
353
1
11.3
31.1

Study Details

Study Description

Brief Summary

Neurocognitive disorders and hypertension occur commonly with aging. While, by definition, older adults are at high cardiovascular risk, there is no guideline exist currently on blood pressure management of elderly hypertension. However, studies have shown that in aging adults, high blood pressure helps prevent against cognitive decline, and low blood pressure on antihypertensive drugs could accelerate it. This study aims at investigating if pharmacological treatment of hypertension in the very elderly is influenced by presence and severity of neurocognitive disorders. Our research hypothesis is that the drug management of hypertension in patients 80 years of age or older more is all the less aggressive as the neurocognitive disorders are advanced.

Condition or Disease Intervention/Treatment Phase
  • Drug: Antihypertensive Agents

Study Design

Study Type:
Observational
Actual Enrollment :
353 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
The Impact of Dementia and Neurocognitive Disorders on Hypertension Treatment in the Very Elderly: the TAHOC Study
Actual Study Start Date :
Jan 1, 2022
Actual Primary Completion Date :
Jan 1, 2022
Actual Study Completion Date :
Dec 12, 2022

Arms and Interventions

Arm Intervention/Treatment
control group

absence of neurocognitive disorder (ND), Mini-Mental State Examination (MMSE) from 27 to 30 inclusive

Drug: Antihypertensive Agents
number of hypertensive drugs

mild neurocognitive disorder

MMSE from 21 to 26 inclusive

Drug: Antihypertensive Agents
number of hypertensive drugs

moderate neurocognitive disorder

MMSE from 11 to 20 inclusive

Drug: Antihypertensive Agents
number of hypertensive drugs

severe neurocognitive disorder

MMSE less than or equal to 10

Drug: Antihypertensive Agents
number of hypertensive drugs

Outcome Measures

Primary Outcome Measures

  1. number of antihypertensive agents [during inclusion]

    among ACEI/ARB2, calcium channel blocker, thiazides and related, central antihypertensive beta blocker

Secondary Outcome Measures

  1. class of antihypertensive medications [during inclusion]

    among ACEI/ARB2, calcium channel blocker, thiazides and related, central antihypertensive beta blocker

  2. systolic and diastolic blood pressure [during inclusion]

    blood pressure measured with upper arm cuffs

  3. orthostatic hypotension [during inclusion]

    a systolic blood pressure decrease of at least 20 mm Hg or a diastolic blood pressure decrease of at least 10 mm Hg within three minutes of standing

Eligibility Criteria

Criteria

Ages Eligible for Study:
80 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • to be 80 years of age

  • with history of hypertension and/or on hypertensive drug(s)

Exclusion Criteria:
  • legal protection measure.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier RĂ©gional Universitaire de Nancy Nancy France 54000

Sponsors and Collaborators

  • Central Hospital, Nancy, France

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pr Athanase BENETOS, principal investigator, Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT05845736
Other Study ID Numbers:
  • 2023PI017
First Posted:
May 6, 2023
Last Update Posted:
May 6, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Pr Athanase BENETOS, principal investigator, Central Hospital, Nancy, France
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2023