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NCT03834844Active, not recruiting

Meditation and Education That is Nurse Delivered for Symptom Management in Paroxysmal Atrial Fibrillation (PAF)

Mindfulness Meditation and Patient Education for Symptom Management in Individuals With Atrial Fibrillation(AF): Do They Need to Be Offered Together?

Source: ClinicalTrials.gov · Last updated 2 Dec 2024

Brief summary (registry, in English)

The aim of this project is to determine whether the entire intervention (Mindfulness meditation, AF education, and weekly phone visits) that is nurse delivered to individuals with paroxysmal atrial fibrillation is more effective than a combination, single or no intervention in the reduction of overall AF symptoms, anxiety, and negative illness perception; or the improvement of quality of life (QOL) and functional status.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
50 (actual)
First submitted
6 Feb 2019
Start date
1 May 2018
Primary completion date
31 Dec 2024
Lead sponsor
Stanford University
NCT number
NCT03834844

What you commit to

  • Study type: Interventional
  • Participants enrolled: 50
  • From 1 May 2018 to the primary completion date, 31 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Hospitalized in prior 3 months for illness other than PAF
  • Previously practiced mindfulness

Other illness

  • Diagnosed with low cardiac function (NYHA Class IV)
  • Cognitive impairment

Other

  • Life expectancy of less than 6 months

Who the study is looking for

  • Individuals with Symptomatic Paroxysmal Atrial Fibrillation
  • A symptomatic episode of PAF within last 6 months
  • 18 years old or greater
  • Able to read and understand English
  • Able to participate in weekly phone calls
  • Able to attend two video visit/phone sessions that are 6 weeks apart

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Stanford Health Care
Coordinator of this site? Confirm its status
StanfordUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.