Ischemic Conditioning to Promote Microvascular Resiliency in Frail Individuals

PHASE2RecruitingINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

May 2, 2023

Primary Completion Date

December 31, 2028

Study Completion Date

December 31, 2029

Conditions
AgingFragilityEndothelial Dysfunction
Interventions
OTHER

Ischemic Conditioning

We will use a randomized block design to randomize individuals into either Ischemic Conditioning-Low or Ischemic Conditioning-High group using an online randomizer. A handheld sphygmomanometer and blood pressure cuff will be given to study participants. For the Ischemic Conditioning-High group participants, while sitting, the cuff will be placed around the non-dominant upper arm and inflated to 225 mmHg for 5 min, then released for a 5-min recovery period. A 5-min inflation period is most used. Five cycles of inflation/recovery will be performed. For the Ischemic Conditioning-Low group participants, the cuff will be inflated to 10 mmHg instead. All participants will perform the intervention daily for 2 weeks. Participants will complete daily log sheets documenting the time and pressure of each cuff inflation.

Trial Locations (1)

53226

RECRUITING

Froedtert Hospital, Wauwatosa

All Listed Sponsors
lead

Medical College of Wisconsin

OTHER