- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06370702
Evaluating the Use of Grip Exercises to Decrease Deep Vein Thrombosis in Adult Patients With PICC Lines
February 12, 2026 updated by: TriHealth Inc.
Patients who have a peripherally-inserted central catheter (PICC) placed are at a risk of developing a deep vein thrombosis (DVT).
At TriHealth, approximately 2-4 patients per month who have a PICC placed experience a subsequent DVT.
One innovative way to possibly mitigate the risk of DVTs is hand grip exercises.
The current study will be the first study to evaluate hand grip exercises for the prevention of DVTs in adult patients hospitalized in the United States.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
2500
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ohio
-
Cincinnati, Ohio, United States, 45242
- Bethesda North Hospital
-
Cincinnati, Ohio, United States, 45220
- Good Samaritan Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Had a PICC placed in the past 24 hours by the Vascular Access Team
- Patient is admitted to either Bethesda North Hospital or Good Samarian Hospital
Exclusion Criteria:
- Under 18 years old
- Does not speak English
- Unable to consent to involvement in the research study
- Has a bleeding disorder/diagnosis
- Has a severe limb disfunction whereby they would be unable to perform the grip exercises
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Handgrip Exercise Group
Participants will be instructed to firmly grip and squeeze the ball for 10 seconds, relax for 10 seconds and repeat for 10 minutes.
They will be instructed to do this 3 times per day.
|
Participants will firmly grip and squeeze the ball for 10 seconds, relax for 10 seconds and repeat for 10 minutes.
They will be instructed to do this 3 times per day.
|
|
No Intervention: Standard Care Group
Participants will receive standard care that includes no instruction about conducting hand grip exercises.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Deep vein thrombosis
Time Frame: from PICC placement to PICC removal, up to 4 weeks
|
Incidence of deep vein thrombosis
|
from PICC placement to PICC removal, up to 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Rachel Baker, PhD, RN, TriHealth Nurse Researcher
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 6, 2023
Primary Completion (Estimated)
May 31, 2027
Study Completion (Estimated)
December 30, 2027
Study Registration Dates
First Submitted
December 19, 2023
First Submitted That Met QC Criteria
April 15, 2024
First Posted (Actual)
April 17, 2024
Study Record Updates
Last Update Posted (Actual)
February 17, 2026
Last Update Submitted That Met QC Criteria
February 12, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 23-054
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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