Viewing Study NCT07489105


Ignite Creation Date: 2026-03-26 @ 3:19 PM
Ignite Modification Date: 2026-03-30 @ 1:21 AM
Study NCT ID: NCT07489105
Status: RECRUITING
Last Update Posted: 2026-03-25
First Post: 2026-03-17
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Forge AHEAD: Feasibility of Yoga to Improve Cognitive Function
Sponsor: Auburn University
Organization:

Study Overview

Official Title: Engaging Stakeholders and Patients to Evaluate the Feasibility of Yoga to Improve Cognitive Function in Rural Heart Failure Patients in the Deep South
Status: RECRUITING
Status Verified Date: 2026-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: Forge AHEAD
Brief Summary: The investigators will conduct a two-phase pilot study to test the feasibility and acceptability of a 12-week Chair Yoga intervention for 20 heart-failure patients. Using a patient-centered approach, investigators will involve stakeholders in designing the protocol, gather patient feedback, and refine the protocol accordingly.
Detailed Description: The aims of this study include:

Phase 1: Engaging stakeholders and patients to develop the initial study protocol.

1. Engage stakeholders and patients to develop the initial study protocol.
2. Recruit the first 10 patients to complete a 12-week online yoga intervention and collect data before and after the yoga intervention.
3. Evaluate the feasibility of yoga intervention and revise the initial study protocol with stakeholders based on the data collected from the patients.

Phase 2: Pilot the revised protocol and finalize plans.

1. Implement the revised study protocol for the next 10 patients, deliver a 12-week online yoga intervention, and collect data before and after the yoga intervention.
2. Evaluate the pilot results on the feasibility of yoga intervention to enhance patient-centered outcomes and cognitive function based on the data collected from the patients.
3. Finalize the study protocol with stakeholders and disseminate findings with communities.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
5P50MD017338-04 NIH None https://reporter.nih.gov/quic… View