Prehabilitation for Aortic Aneurysm Surgery: Proof-of-concept Trial
Purpose
This is a single-arm, proof-of-concept trial to examine the feasibility, acceptability, and preliminary efficacy of the Ready for Recovery program, a 6-week collaborative care intervention to help prepare individuals for repair of aortic aneurysms.
Condition
- Aortic Aneurysm
 
Eligibility
- Eligible Ages
 - Over 18 Years
 - Eligible Sex
 - All
 - Accepts Healthy Volunteers
 - No
 
Inclusion Criteria
- Adults undergoing elective aortic aneurysm repair (open or endovascular)
 
Exclusion Criteria
- Cognitive disturbance - Current pregnancy or plan to become pregnant prior to surgery - Inability to write/speak fluently in English
 
Study Design
- Phase
 - N/A
 - Study Type
 - Interventional
 - Allocation
 - N/A
 - Intervention Model
 - Single Group Assignment
 - Primary Purpose
 - Prevention
 - Masking
 - None (Open Label)
 
Arm Groups
| Arm | Description | Assigned Intervention | 
|---|---|---|
| 
                        Experimental Ready for Recovery  | 
                    Participants in this arm will receive the Ready for Recovery intervention. | 
                                                
  | 
                
Recruiting Locations
Boston 4930956, Massachusetts 6254926 02155
More Details
- Status
 - Recruiting
 - Sponsor
 - Massachusetts General Hospital
 
Detailed Description
This is a single-arm, proof-of-concept trial to examine the feasibility, acceptability, and preliminary efficacy of the Ready for Recovery program. Ready for Recovery is a 6-week collaborative care program to prepare individuals for surgical procedures to repair an aortic aneurysm. Participants will speak with a study trainer on the phone each week and will set goals related to physical activity, a healthy diet, and inspiratory muscle training. They also will be given resources to reduce stress, treat anxiety and depression (if present), and stop smoking, and the study team will make recommendations regarding medication adjustments to reduce complications after surgery. The primary outcome is feasibility (measured by percentage of phone sessions completed). Secondary outcomes include acceptability (measured by weekly 0-10 utility ratings) and preliminary impact on functional, psychological, and health behavior outcomes.