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Training of Arms to Reduce Pain With Peripheral Venous Catheter

V

Vejle Hospital

Status

Terminated

Conditions

Veins
Cancer
Pain

Treatments

Other: Arm training

Study type

Interventional

Funder types

Other

Identifiers

NCT05716217
Vein-project

Details and patient eligibility

About

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.

Enrollment

9 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

9 participants in 2 patient groups

Training group
Experimental group
Treatment:
Other: Arm training
Normal care
No Intervention group

Trial contacts and locations

1

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Central trial contact

Agnete Kaltoft, MHSc; Hanne I Jensen, PhD

Data sourced from clinicaltrials.gov

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