Recruiting

Observational Study

Sponsor:

Yale University

Code:

NCT05743673

Conditions

Perioperative/Postoperative Complications

Aerobic Capacity

Eligibility Criteria

Sex: All

Age: 60+

Healthy Volunteers: Accepted

Interventions

Shape II

Study Details

Brief summary:

This study is looking at whether a simplified exercise test called the SHAPE-HF cardiopulmonary testing system can be used before surgery in older adults. Doctors often need to know how well a patient's heart, lungs, and body handle physical activity before moderate- to high-risk surgery. This information may help them better understand a patient's fitness for surgery and possible risk of complications afterward.

The study will enroll adults older than 60 years who are being evaluated before planned moderate- to high-risk noncardiac surgery. The first goal is to determine if this was feasible in older adults and to learn whether patients can be successfully recruited to complete this pre-surgery test. Secondly, the study will also look at how results from the SHAPE-HF system compare with common ways doctors now estimate fitness, such as asking patients about their physical activity and using a standard questionnaire.

Participants will attend one in-person study visit lasting about 35 minutes. During that visit, they will answer questions about their activity level and complete testing with the SHAPE-HF system. The test uses short periods of lower-intensity exercise to estimate aerobic fitness. After the visit, participants will be contacted by phone about 24 hours later to check for any problems related to the study test.

Lastly, researchers will also review information from the medical record for 30 days after surgery to see whether test results are related to recovery, short-term health problems after surgery, or major complications. No extra surgery or change in planned medical care is part of this study. The information learned may help improve how doctors evaluate older adults before surgery in the future.

Conditions

Perioperative/Postoperative Complications

Aerobic Capacity

Study ID

NCT05743673

Start date

May 3, 2023

Status verified date

Apr, 2026

Completion date

May 29, 2026

Anticipated

Primary completion date

May 29, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 60+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Aged >60 years
  • Scheduled for pre-surgical evaluation for moderate to high-risk surgical procedure.
  • RCRI <2 based on screening of preoperative co-morbidities.
  • Provision of signed and dated informed consent form

Exclusion Criteria:

1. Age <60 years old
2. Subjective METS <4
3. Inability to give independent informed consent
4. Revised Cardiac Risk Index (RCRI) >2
5. Neurological impairment with motor limitations
6. Mental impairment leading to inability to cooperate
7. Recent NSTEMI or STEMI type myocardial infarction (within 6 months)
8. Angina (stable or unstable, within 6 months)
9. Uncorrected severe valvular heart disease (severe aortic, tricuspid, or mitral stenosis)
10. Recent exacerbation of congestive heart failure (requiring hospitalization, within 6 months)
11. Acute pulmonary embolism or deep vein thrombosis (within past 6 months)
12. Uncontrolled pulmonary edema
13. Uncontrolled symptomatic arrhythmias
14. Active endocarditis
15. Acute myocarditis or pericarditis
16. Active wheezing or home oxygen use
17. Recent exacerbation of chronic obstructive pulmonary disease or asthma or pneumonia (requiring hospitalization, within 6 months)
18. Inability to perform components of the SHAPE test (severe hip flexion limitation, severe osteoarthritis of knee or hip, limb immobilization, ambulation with a walker, can or crutches, baseline balance irregularities
19. Diagnosis of vertigo
20. Known allergic reactions to components of the SHAPE medical system apparatus disposable mouthpiece.
21. Active enrollment in an interventional clinical trial within the enrollment period of the study.

Study Design

Enrollment

371 participants

Anticipated

Interventions and Outcome Measures

Arms

Validation Cohort

Older subjects (>60 years old) presenting for moderate to high-risk surgical procedure with reported subjective metabolic equivalents of >4 METS and with a score of <4 on the revised cardiac risk index (RCRI) undergoing submaximal exercise testing.

Interventions

Shape II

cardiopulmonary exercise testing apparatus

Primary outcome measure

  • Recruitment Success [ Time Frame: 0-30 days ]

Central Contacts and Locations

Central contacts

Locations

Yale New Haven Hospital

Recruiting

New Haven, Connecticut, United States, 06520

More Information

Sponsor

Yale University

Last update posted

May 7, 2026

Last verified

Apr, 2026

Keywords

  • perioperative risk stratification
  • submaximal cardiopulmonary exercise testing
  • postoperative complications
  • perioperative complications

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Yale University on 2026-05-07.