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Atrial FibrillationDIAL-FNCT01816308

Cognitive Impairment in Atrial Fibrillation

An observational study of Atrial Fibrillation and Mild Cognitive Impairment, run by Texas Cardiac Arrhythmia Research Foundation at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This study aims to compare the incidence of new-onset cognitive impairments and change in existing impairment status between AF patients undergoing either catheter ablation or remaining on anti-arrhythmic drugs (AAD) as assessed by Montreal Cognitive Assessment (MoCA). Read more about this study

Who is it for?
Ages 50 to 75 years
How many people
888 participants
Where
1 siteUnited States
Study dates
Jul 2014to Dec 2022
How long will I take part?
2 Years
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Detail study information will be provided to the patients and written informed consent will be obtained from the each patient or family member before enrolling in the study. Consenting patients will be evaluated and the appropriate treatment strategy for managing arrhythmia will be independently determined by the physicians at the participating centers. Patients undergoing catheter ablation for AF will be included in the study group and those determined to stay on AAD will form the control group.

Who may be able to join

  • Age: ≥ 50 years, male or female subjects
  • Clinical diagnosis of AF
  • Ability to provide written, informed consent

Who cannot join

  • Patients with established dementia
  • MoCA score ≤ 17 on Montreal Cognitive Assessment (MoCA)
  • Use of illicit drugs
  • Alcohol use: >12 drinks/week on average
  • Clinical evidence of delirium or altered mental status
  • Medically unstable patients (acute/unstable or poorly controlled problems that would demand focused, relatively urgent or emergent medical attention)

Trial locations and contacts

1 site in 1 country.

United States1 site, 1 recruiting
  • Texas Cardiac Arrhythmia Institute, St. david's Medical Center

    Austin, Texas, 78705

    Mitra Mohanty, MD, 512-544-8198, mitra.mohanty@stdavids.com

    Recruiting

Other trials in United States

About this study

Official title: Mild Cognitive Impairment (MCI) in Patients With Atrial Fibrillation (AF), Trajectories of the Progression of MCI and Factors Associated With the Progression

This study aims to compare the incidence of new-onset cognitive impairments and change in existing impairment status between AF patients undergoing either catheter ablation or remaining on anti-arrhythmic drugs (AAD) as assessed by Montreal Cognitive Assessment (MoCA).

Read the detailed description

Background: AF is mostly a disease of elderly. Up to 10% of people aged 80 years or older suffer from this arrhythmia and the rate is projected to triple in the next 20 years (1). Evidence is emerging that AF may increase the risk of all forms of dementia (2). Cerebral hypoperfusion and the risk of cerebrovascular micro- and macro-embolism are plausible explanations for the predisposition for cognitive decline in AF (1). Such insults may act alone or in concert with other neuropathological changes common in the brain of older individuals such as neuritic plaques or neurofibrillary tangles, in lowering cognitive reserves and accelerating the onset of dementia (3).

Prior studies on AF and dementia have yielded conflicting results.

An earlier study provided evidence supporting an association between AF and increased incidence of dementia in patients with stroke (4). In a prospective study conducted on participants of ONTARGET and TRANSCEND trials, it was revealed that cognitive and functional decline are important consequences of atrial fibrillation, even in the absence of overt stroke (5). Another independent study, observed similar results for risk of dementia in AF in participants with and without clinically recognized stroke during follow-up (3). Evidences from a previous research demonstrated not only a significant association of AF with all forms of dementia including Alzheimer's disease, but also higher mortality rate in patients with coexistent dementia and AF (2). On the contrary, some studies did not find any significant risk-association between AF and dementia (6-8).

These contradictory results compel the necessity for a prospective study on a large population to obtain a clear understanding of the association between AF and cognitive impairment. The potential association between the two conditions can have a very important clinical implication; if there were a causal relationship between AF and dementia then the different therapeutic strategies of AF may have differing influence on dementia risk (3). Thus, this knowledge would facilitate in personalizing treatment approaches for individuals with AF.

Anti-arrhythmic drugs are considered as the first line of therapy in AF and catheter ablation is widely-recognized as the best option in drug-refractory cases. Recent published data suggested that effective rhythm-control by catheter ablation reverses the risk of dementia in AF (9). However, it was an epidemiologic study from a health-care database where ICD codes were used to identify clinical dementia. Therefore, mischaracterization of the dementia subtypes was a major possibility in their study.

None of the other currently ongoing studies or registries on AF ablation in US includes dementia as one of the outcomes to be assessed. Therefore, our study will be the first to examine the benefit of successful catheter ablation on cognitive function in AF patients by directly assessing cognition using standardized instruments.

There are several standardized screening tools available to assess cognitive status, namely Mini-Mental State Examination (MMSE), Cognitive Abilities Screening Instrument (CASI) and Montreal cognitive assessment (MoCA). All have their strengths and limitations, but MoCA is considered the most efficient because of its cross-cultural applicability and its higher sensitivity for detecting mild cognitive impairments. In our study, MoCA would be used to evaluate cognitive status in AF patients.

Besides MoCA, the following questionnaires will be used to assess other risk-factors for cognitive impairment and quality of life in AF patients

  1. Hospital anxiety and Depression scale (HAD): to evaluate anxiety and depression
  2. Katz Index of Independence in Activities of Daily Living (ADL) and Lawton's Instrumental Activities Of Daily Living Scale (IADL): to assess independent living skills
  3. Multidimensional Scale of Perceived Social Support by Zimet et al: to appraise perception of social-support in this study
  4. International Physical Activity Questionnaire (IPAQ): to obtain internationally comparable data on health-related physical activity
  5. Atrial Fibrillation Effect on Quality-of-Life (AFEQT) questionnaire: to assess the AF-specific changes in QoL before and after ablation

Study Objectives

Primary Objectives:

To evaluate the number of patients showing improvement or no-worsening in cognitive status at 2 years follow-up after catheter ablation or after the beginning of drug-therapy in non-ablation group

Secondary Objectives:

  1. Study the interaction between depression, social support and cognitive status
  2. Evaluate the impact of social supports on the trajectory of dementia
  3. Examine the correlation between physical activity and cognitive impairment
  4. Assess the impact of arrhythmia recurrence on dementia across the control and the study group

Study Design:

This prospective multicenter study will enroll 888 consecutive AF patients at different centers in US, Asia and Europe.

Consenting patients will perform the MoCA evaluation. Patients with a score < 17 will be deemed a screen failure. Qualifying patients will be evaluated and the appropriate treatment strategy for managing arrhythmia will be independently determined by the treating physician. Patients undergoing a clinically indicated catheter ablation for AF will be assigned to the Ablation group and those determined to stay on AAD will form the AAD group. Based on physician decision, left atrial appendage occlusion or exclusion procedures may be performed for reducing the thromboembolic risk. The AAD group will continue on AADs as prescribed in accordance with standard of care at the discretion of the physician.

Keywords
AF, MCI
Medical subject headings
Atrial Fibrillation, Cognitive Dysfunction, Dementia

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. improvement or no-worsening in MoCA score assessed at baseline and 2 year follow-up

    The primary efficacy endpoint of this study will be the objective response rate (ORR); objective response being defined as improvement or no-worsening in MoCA score assessed at baseline and 2 year follow-up.

    Measured: 2 years

Secondary outcomes (1)
  1. Correlation between MoCA score and physical activity, social support, anxiety and depression

    1. Correlation of scores between the HAD and the social support scale
    2. Correlation of scores between HAD and MoCA
    3. Association between social support and MoCA score
    4. Correlation between physical activity and MoCA scale
    5. Association between arrhythmia recurrence and MoCA score
    6. Comparison of QoL between baseline and post-ablation period

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Mar 2013 (estimated)
  2. Study startJul 2014
  3. Primary completionJun 2020 (estimated)
  4. Study completionDec 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
888 participants (estimated)
Target duration
2 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT01816308
Sponsor's protocol ID
TCAI_DIAL-F
Acronym
DIAL-F
Status last verified
Sep 2019
First submitted
20 Mar 2013
Last updated
9 Sep 2019
Results posted
No
Data monitoring committee
No

Publications

  • Mohanty S, Mohanty P, Trivedi C, Assadourian J, Mayedo AQ, MacDonald B, Della Rocca DG, Gianni C, Horton R, Al-Ahmad A, Bassiouny M, Burkhardt JD, Di Biase L, Gurol ME, Natale A. Impact of Oral Anticoagulation Therapy Versus Left Atrial Appendage Occlusion on Cognitive Function and Quality of Life in Patients With Atrial Fibrillation. J Am Heart Assoc. 2021 May 4;10(9):e019664. doi: 10.1161/JAHA.120.019664. Epub 2021 Apr 19.

    PubMed 33870705

Questions about this trial

What is this clinical trial studying?

An observational study of Atrial Fibrillation and Mild Cognitive Impairment, run by Texas Cardiac Arrhythmia Research Foundation at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 9 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Mitra Mohanty, MD (512-544-8198, mitra.mohanty@stdavids.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

improvement or no-worsening in MoCA score assessed at baseline and 2 year follow-up (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01816308, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2019.

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