Portable Resistance Exercise For Strength And Stability – Lung Transplant (PRESS-LT)
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Scottsdale/Phoenix, Arizona: 26-008950
- Jacksonville, Florida: 26-008950
- Rochester, Minnesota: 26-008950
About this study
The purpose of this study is to evaluate the feasibility of consistently applying therapist-directed progressive lower-extremity resistance training during the immediate post–lung transplant inpatient recovery period across participating Mayo Clinic sites.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
Adult lung transplant recipient during index admission.
Medically cleared for PT/OT activity by the primary team.
Demonstrates functional limitation appropriate for inpatient rehabilitation intervention.
Able to participate in therapist-directed strengthening at the lowest clinically appropriate intensity.
Agreeable to participate in strengthening intervention and research procedures, as required by the final regulatory pathway.
Has baseline functional status measurable using AM-PAC and/or other prespecified PT/OT outcomes.
Exclusion Criteria:
Hemodynamic or respiratory instability precluding therapy participation.
Contraindication to resistance training per PT/OT, surgical, or medical precautions.
Conditions when participation is not clinically appropriate, such as ECMO, intubation, open chest, unstable vasoactive medication requirements, lower-extremity injury or wound with weight-bearing restriction, severe delirium preventing participation, or refusal of research consent.
Major neurologic event preventing meaningful participation in the intervention or outcome assessment.
Immediate planned transfer to inpatient rehabilitation or discharge within 24 hours when insufficient time remains for baseline assessment and intervention exposure.
Note: Other protocol defined Inclusion/Exclusion Criteria may apply.
Eligibility last updated 09/01/2026. Questions regarding updates should be directed to the study team contact.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Scottsdale/Phoenix, Ariz.
Mayo Clinic principal investigator James Craigo, APRN, C.N.P., M.S.N. |
Contact us for the latest status |
|
Jacksonville, Fla.
Mayo Clinic principal investigator Sheri Dingman, P.T., D.P.T. |
Contact us for the latest status |
|
Rochester, Minn.
Mayo Clinic principal investigator Elizabeth Olsen, APRN, C.N.P., M.S.N. |
Contact us for the latest status |
|
More information
Publications
Publications are currently not available