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Training of Arms to Reduce Pain With Peripheral Venous Catheter

Can Training of the Armsy Reduce Pain When Inserting a Peripheral Venous Catheter, and How is it Experienced That There Can be Challenges With Vein Status for Patients in Cytostatic Treatment?

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05716217
Enrollment
9
Registered
2023-02-08
Start date
2023-02-28
Completion date
2024-04-16
Last updated
2024-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Cancer, Veins

Brief summary

Female patients undergoing chemotherapy for breast cancer often experience pain and discomfort when a peripheral venous catheter is inserted. This randomized, controlled trial investigates whether there is a difference in the degree of pain during PVC insertion in patients who exercise their arms, and whether exercise improves vein status. Participation involves: * Everyone must have had their peripheral venous catheter (PVC) inserted at least five times in the DROP-IN, which is an outpatient clinic staffed by anesthesia nurses who are specialists in applying PVCs. * Everyone will three times be asked to answer some questions in the DROP-IN, have their grip strength measured in both hands, and have the course of the veins in their arms clarified. * The training group must do arm training exercises daily for at least eight weeks (training equipment is provided) * Ten participants will at the end of the project period be invited to participate in a telephone interview about experiences of vein status during a cancer treatment course.

Interventions

Daily arm training program

Sponsors

Vejle Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Masking description

The anaesthesia nurses inserting PVCs and registering data are blinded to the participants' study allocation.

Intervention model description

One group is randomly assigned to an 8-week daily arm training program. The other group receives normal care

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Planned neoadjuvant or adjuvant chemotherapy via intravenous peripheral venous cannula placed under ultrasound guidance * PVC insertion is performed in the DROP-IN outpatient clinic, Department of Anesthesiology, Vejle Hospital, at least four times * The patient has provided written and orally informed consent * The patient must be cognitively well preserved and able to understand information

Exclusion criteria

* Patients who cannot read and understand Danish * Patients \<18 years

Design outcomes

Primary

MeasureTime frameDescription
Level of pain as measure by the Numeric Rating Scale (score 1-10 where a low value defines low level of pain)Measured at baselinePain level after insertion of periphral venous catheter and at general activity measured with Numeric Rating Scale

Secondary

MeasureTime frameDescription
Vein statusMeasured at baselineNumber of useable veins (assessed via ultrasound)

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026