Assessing Connected-Health, Pressure-Monitoring Technology for Improving Compression Therapy in Venous Leg Ulcer Treatment
Feeltect Limited · with Parkview Health · NCT07152717
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 40
- US sites recruiting
- 1
- Study start
- November 6, 2025
- Record last updated
- September 9, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study evaluates the effectiveness of a connected-health, pressure monitoring technology (Tight Alright) to improve clinical outcomes of compression therapy in patients with venous leg ulcers (VLUs). Compression therapy is the standard of care for VLUs, but achieving and maintaining therapeutic sub-bandage pressure is challenging due to patient variability and lack of objective feedback. The Tight Alright system includes a wearable device that measures sub-bandage pressure at multiple points on the leg and transmits data to a mobile app and cloud database, enabling both guided compression application at the point-of-care and guided compression maintenance via remote monitoring.
The study will be conducted at Parkview Noble Center for Wound Healing and will include two cohorts: a control group receiving standard unguided compression therapy with blinded device use (i.e. compression pressures will be blinded at the point of care but monitored remotely), and an intervention group using Tight Alright technology to guide compression application and reapplication. Outcomes will include wound healing rates, time to healing, pressure maintenance, patient adherence, and usability. The study aims to determine whether integrating connected-health pressure monitoring can improve consistency of compression therapy, accelerate healing, and enhance patient engagement in the treatment of venous leg ulcers
Being studied: A connected-health, pressure-sensing system for monitoring sub-bandage pressure during compression therapy
Conditions: Venous Leg Ulcers (VLUs)
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Patient of Parkview Noble Center for Wound Healing
- Adults 18+ with venous leg ulcers receiving compression therapy treatment prescribed by outpatient wound clinic.
- Capable of using use a smart device
- Owns a smart phone or device capable of downloading the Mobile App
Exclusion Criteria
- \<18 years old
- Unable to consent in English
- Cellulitis in affected limb
- Acute deep vein thrombosis in affected limb
- Active malignancy in affected limb
- Prisoners
- Currently enrolled in or has been enrolled in another investigation device or drug trial in the last 30 days
Recruiting US locations
Parkview Center for Wound Healing
Fort Wayne, IN 46805
Study contacts (from the official record)
- Brooke Randol, MSN, RN, AGCNS-BC, CMSRN, CWS · (260) 347-8610 · Brooke.randol@parkview.com