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Forge AHEAD: Feasibility of Yoga to Improve Cognitive Function

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
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07489105
Acronym
Forge AHEAD
Enrollment
20
Registered
2026-03-23
Start date
2025-07-24
Completion date
2027-12-31
Last updated
2026-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Rural Health, Engagement, Patient

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.

Interventions

BEHAVIORALYoga group

Chair yoga intervention

Sponsors

Auburn University
Lead SponsorOTHER
National Institute on Minority Health and Health Disparities (NIMHD)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Heart failure diagnosis * Aged 55 years or older

Exclusion criteria

* Traumatic brain injury, co-existing neurological and psychiatric disorders * Implanted defibrillator or metal objects, left ventricular assist device placement, or cardiac transplant * Substance abuse * Unable to perform yoga due to physical limitations or severity of illness * Currently engaged in a yoga program

Design outcomes

Primary

MeasureTime frameDescription
Perceptions and experiences of yoga practice measured by the Essential Properties of Yoga Questionnaire.After completion of 12-week intervention.Includes 62 items. Rated on Likert scales from 0 (not at all) to 4 (a very large amount). Score range converted to 0 to 100%, with higher scores indicating a stronger presence/intensity of the specific yoga property.
Cognitive function measured by the Montreal Cognitive Assessment.BaselineScore range 0 to 30. Score ≥26: generally normal (context-dependent); 18-25: mild impairment range; \<18: more likely moderate-severe impairment.

Secondary

MeasureTime frameDescription
Health-related quality of life measured by the Minnesota Living with Heart Failure Questionnaire.Change from 0-12 weeks, from baseline pre-intervention to 12 weeks post-intervention.Response scale: 0 (no impact) to 5 (very much). Score ranges from 0 to 105, with higher scores indicating worse quality of life.
Social factors of health measured by the Protocol for Responding to and Assessing Patients' Assets, Risks, and Experiences.BaselineFor each PRAPARE item, mark responses indicating unmet social need as "1" (risk) and acceptable/no-need responses as "0." Scores are calculated by summing each item; higher scores indicate more social needs.

Countries

United States

Contacts

CONTACTChin-Yen Lin, PhD, RN
czl0194@auburn.edu334-844-5619

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026