RECRUITING

The Z Stitch Early Bed Rest Assessment Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this study is to understand the effects of early mobilization after a Z stitch procedure in patients undergoing certain heart-related treatments. The investigators want to find out if allowing patients to move around sooner after their procedure can improve their satisfaction and potentially lead to earlier discharge from the hospital. Type of Study: Clinical Trial Participant Population/Health Conditions: Patients aged 18-99 undergoing specific heart procedures such as atrial fibrillation treatment, atrial flutter treatment, supraventricular tachycardia treatment, diagnostic electrophysiology studies, AV node ablation, or Watchman device placement. Main Questions: Does early mobilization (getting up and moving around sooner) after the Z stitch procedure improve patient satisfaction? Participants will be divided into two groups, and researchers will compare those who have one hour of bedrest with those who have four hours of bedrest after the Z stitch procedure. The investigators want to see if the shorter bedrest period leads to higher patient satisfaction.

Official Title

The Z Stitch Early Bed Rest Assessment Study

Quick Facts

Study Start:2024-01-01
Study Completion:2025-05-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06087497

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Atrial fibrillation
  2. * Atrial flutter
  3. * Supraventricular tachycardia
  4. * Diagnostic EP study
  5. * Atrioventricular node ablation
  6. * Watchman device placement
  1. * Those who refuse or are unable to consent.
  2. * Cases involving arterial access.
  3. * Cases involving access with a \>16Fr sheath (i.e., no leadless pacer patients).
  4. * Patients with a BMI \> 40.
  5. * Lead-extraction patients.

Contacts and Locations

Study Contact

Adarsh Katamreddy, MD
CONTACT
503 494 7400
katamred@ohsu.edu
Charles Henrikson, MD
CONTACT
503 494 7400
henrikso@ohsu.edu

Principal Investigator

Charles Henrikson, MD
PRINCIPAL_INVESTIGATOR
Oregon Health and Science University

Study Locations (Sites)

Oregon Health and Science University
Portland, Oregon, 97239
United States
Portland VA Medical Center
Portland, Oregon, 97239
United States

Collaborators and Investigators

Sponsor: Oregon Health and Science University

  • Charles Henrikson, MD, PRINCIPAL_INVESTIGATOR, Oregon Health and Science University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-01
Study Completion Date2025-05-01

Study Record Updates

Study Start Date2024-01-01
Study Completion Date2025-05-01

Terms related to this study

Additional Relevant MeSH Terms

  • Atrial Fibrillation
  • Atrial Flutter
  • Supraventricular Tachycardia
  • Syncope
  • Ventricular Tachycardia