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Recruiting

NCT Number: NCT07659015

Use of Hand Extension Rubber During Intravenous Catheter Placement

The study aims to investigate the effect of a hand extension rubber used in patients with peripheral intravenous catheters on pain, anxiety, and satisfaction.

Recruiting

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

While the use of non-pharmacological methods to reduce pain and anxiety levels and increase satisfaction during peripheral intravenous catheterization has gained importance in recent years, studies on techniques that are easy to implement, low-cost, and proven to be effective-particularly in adults-remain limited. It is believed that the hand extension rubber has the potential to reduce pain and anxiety as a distraction method, thereby increasing patient satisfaction. The findings will enhance nurses' adherence to evidence-based practices and improve the quality of patient care. This study holds unique value as it is the first research in Turkey to address this method in adult individuals.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Volunteers willing to participate in the study
  • Patients aged 18-65
  • Patients who are alert and able to communicate verbally in Turkish
  • Patients assigned to the green zone during triage
  • Patients suitable for PICC placement in the left cephalic and basilic veins
  • Patients who are right-handed
  • Patients with a VAS pain score of 0 prior to the PIC procedure

Exclusion criteria

  • Patients with acute or chronic pain
  • Patients with conditions that cause limited mobility, such as muscle disorders or grip dysfunction
  • Patients with peripheral neuropathy, arteriovenous fistula, or bilateral mastectomy
  • Patients with a psychiatric diagnosis (as self-reported)
  • Patients with communication impairments (hearing, speech, and vision)
  • Patients with a history of negative PIC procedure experiences

Terminating Criteria:

  • Participants wishing to withdraw from the study at any stage after giving their consent
  • Failure of the PIC procedure
  • Failure to use the hand extension band until the end of the procedure
  • Occurrence of complications related to the PIC procedure during the procedure

Treatment and study plan

Hand Extension Rubber

Other

Hand Extension Rubber will be used for distraction while peripheral IV catheher placement.

Primary outcomes

  1. Pain associated with PIC procedure (using VAS-visual analogue scale)

    Time frame: after the PIC implementation

    Pain associated with PIC procedure

Secondary outcomes

  1. satisfaction associated with PIC procedure (using State-Trait Anxiety Inventory)

    Time frame: after the PIC implementation

    satisfaction

  2. anxiety associated with PIC procedure (using a five likert type quesiton-)

    Time frame: after the PIC implementation

    anxiety

Study contacts

Contact information is provided by the study sponsor or research team.

Gülden Basit

CONTACT

[email protected]

+90 332 320 40 29

Melike Kışla

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Necmettin Erbakan University

Other

Collaborators

  • Konya Necmettin Erbakan Üniversitesi

Registry information

Official study title

The Effect of Hand Extension Rubber Used in Patients With Peripheral Intravenous Catheter Insertion on Pain, Anxiety and Satisfaction: A Randomized Controlled Trial

Acronym: PIC

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 22, 2026
Registry last updated
Jun 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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