Peripheral Venous Catheter and Masking Tape

NCT05264844 | Completed

• 1 other identifier: 123456
• Study Type: interventional
• Target: 70
• Locations: 1 country
• Sites: 1

Brief Summary

urpose: This study will be carried out to determine the effect of two different catheter covers on the comfort, satisfaction, pain level of the patient and the satisfaction of the nurse. Materials and Methods: This study, which is planned as an open-label randomized controlled post-test study, will be carried out between December 2021 and February 2022. Data; Descriptive Properties will be collected with the Information Form and Visual Analog Scale (Visual Analog Scale-VAS). Data will be collected face to face by researchers.

Conditions

Personal Satisfaction; Pain; Comfort

Keywords

Peripheral venous catheter; chemotherapy; patch; fixation

Outcome Measures

Primary Outcomes (3)

• Pain level

  To be evaluated with "Visual analog scale"

  a week

• Patient comfort

  To be evaluated with "Visual analog scale"

  a week

• Nurse's practice satisfaction

  To be evaluated with "Visual analog scale"

  a week

Study Arms (2)

masking tape group

EXPERIMENTAL

Masking tape will be used

Other: Masking tape

standard catheter dressing group

NO INTERVENTION

Medical plaster to be used (It is routine practice in the clinic.)

Interventions

Masking tape OTHER

IV catheters will be fixed with masking tape

masking tape group

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Being between the ages of 18-65
• Being open to communication and cooperation
• Being conscious and able to answer questions
• Volunteering for research
• Being receiving chemotherapy treatment with a peripheral venous catheter

You may not qualify if:

• Having a disease that may affect the ability to make decisions (dementia, psychological disorders, etc.)
• Having sensory losses such as vision and hearing
• Being in terminal period

Sponsors & Collaborators

• Necmettin Erbakan University: lead

Study Sites (1)

Necmettin Erbakan Univercity

Konya, 42370, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Personal Satisfaction; Pain

Condition Hierarchy (Ancestors)

Behavior; Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Masking Details: Only the statistician will be masked
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Model Details: Randomized controlled trial

Study Record Dates

• First Submitted: January 19, 2022
• First Posted: March 3, 2022
• Study Start: May 1, 2022
• Primary Completion: August 1, 2022
• Study Completion: September 20, 2022
• Last Updated: February 2, 2023

Record last verified: 2023-02

Locations

TU (1)