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NCT Number: NCT07808632

Effect of Stress Ball Use During Femoral Arterial Sheath Removal After Coronary Angiography

This randomized controlled trial aims to evaluate the effects of stress ball use during femoral arterial sheath removal after coronary angiography on pain, anxiety, patient satisfaction, and hemodynamic parameters. A total of 34 patients will be randomly assigned in a 1:1 ratio to either the intervention group or the control group. Participants in the intervention group will use a stress ball during femoral arterial sheath removal in addition to routine care, while participants in the control group will receive routine care only. Pain, anxiety, patient satisfaction, and hemodynamic parameters will be assessed before and at specified time points after femoral arterial sheath removal.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Turkey, Mersin University Hospital

Yenişehir, Mersin, 33120, Turkey (Türkiye)

Location contact

Tuğba ÇAM YANIK

CONTACT

[email protected]

05067703216

About this study

Coronary angiography is a commonly used invasive procedure for the diagnosis and treatment of coronary artery disease. Following coronary angiography performed via the femoral artery, removal of the femoral arterial sheath may cause pain and anxiety and may lead to changes in hemodynamic parameters. Therefore, simple, safe, and nonpharmacological nursing interventions that can improve patient comfort during femoral arterial sheath removal are important.

This prospective, two-arm, randomized controlled trial aims to evaluate the effects of stress ball use during femoral arterial sheath removal after coronary angiography on pain, anxiety, patient satisfaction, and hemodynamic parameters. The study will include 34 patients who meet the eligibility criteria. Participants will be randomly assigned in a 1:1 ratio to either the stress ball intervention group (n=17) or the control group (n=17) using block randomization.

Participants assigned to the intervention group will receive a stress ball immediately before femoral arterial sheath removal. A round, medium-firm silicone stress ball approximately 6 cm in diameter will be used. Participants will be instructed to hold the stress ball in their hand and rhythmically squeeze and release it after counting to three. The intervention will begin approximately one minute before femoral arterial sheath removal and will continue during and after sheath removal for a total of 10 minutes. Participants in the control group will receive routine clinical care without any additional nonpharmacological intervention.

Pain intensity will be assessed using the Visual Analog Scale (VAS), anxiety using the Visual Analog Scale for Anxiety (VAS-A), and patient satisfaction using the Visual Analog Scale for Patient Satisfaction (VAS-PS). Hemodynamic parameters will include systolic blood pressure, diastolic blood pressure, heart rate, respiratory rate, and peripheral oxygen saturation (SpO2).

Assessments will be performed at five predefined time points: immediately before femoral arterial sheath removal (T0), immediately after sheath removal (T1), and at 5 minutes (T2), 15 minutes (T3), and 30 minutes (T4) after the procedure. Routine medical treatment and nursing care will be continued for participants in both groups throughout the study.

The primary outcome of the study is pain intensity associated with femoral arterial sheath removal. Secondary outcomes include anxiety, patient satisfaction, systolic and diastolic blood pressure, heart rate, respiratory rate, and peripheral oxygen saturation. The findings are expected to provide evidence regarding the effectiveness of stress ball use as a simple, low-cost, noninvasive nursing intervention during femoral arterial sheath removal after coronary angiography.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients who underwent coronary angiography via the femoral artery and received stent implantation or balloon angioplasty
  • Aged 18 years or older
  • Willing to participate in the study and providing written informed consent
  • Conscious, oriented, and cooperative
  • Able to read and understand Turkish
  • No hearing or visual impairment that would interfere with participation
  • Clinically and hemodynamically stable
  • No diagnosed psychiatric disorder

Exclusion criteria

  • Coronary angiography performed via the radial artery
  • Development of a complication during coronary angiography, such as arrhythmia
  • Administration of sedation during coronary angiography
  • Pregnancy
  • Prisoners or other vulnerable individuals

Treatment and study plan

stress ball

Behavioral

Participants will be given a round, medium-firm silicone stress ball approximately 6 cm in diameter. They will be instructed to hold the stress ball in the palm of their hand and rhythmically squeeze and release it after counting to three. The intervention will begin approximately one minute before femoral arterial sheath removal and will continue during and after sheath removal for a total of 10 minutes. Routine clinical care will continue throughout the intervention.

Primary outcomes

  1. Pain Intensity

    Time frame: Immediately before femoral arterial sheath removal, immediately after removal, and 5, 15, and 30 minutes after removal.

    Pain intensity will be assessed using a 10-cm Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (worst possible pain). Higher scores indicate greater pain intensity.

Secondary outcomes

  1. Anxiety Level

    Time frame: Immediately before femoral arterial sheath removal, immediately after removal, and 5, 15, and 30 minutes after removal.

    Anxiety will be assessed using the Visual Analog Scale for Anxiety (VAS-A), a 10-cm scale ranging from 0 (no anxiety) to 10 (highest possible anxiety). Higher scores indicate greater anxiety.

  2. Patient Satisfaction

    Time frame: Immediately before femoral arterial sheath removal and 30 minutes after removal.

    Patient satisfaction will be assessed using the Visual Analog Scale for Patient Satisfaction (VAS-PS), a 10-cm scale ranging from 0 (not satisfied at all) to 10 (completely satisfied). Higher scores indicate greater patient satisfaction.

  3. Systolic Blood Pressure

    Time frame: Immediately before femoral arterial sheath removal, immediately after removal, and 5, 15, and 30 minutes after removal.

    Systolic blood pressure will be measured using a bedside patient monitor and recorded in millimeters of mercury (mmHg).

  4. Diastolic Blood Pressure

    Time frame: Immediately before femoral arterial sheath removal, immediately after removal, and 5, 15, and 30 minutes after removal.

    Diastolic blood pressure will be measured using a bedside patient monitor and recorded in millimeters of mercury (mmHg).

  5. Heart Rate

    Time frame: Immediately before femoral arterial sheath removal, immediately after removal, and 5, 15, and 30 minutes after removal.

    Heart rate will be measured using a bedside patient monitor and recorded as beats per minute (beats/min).

  6. Respiratory Rate

    Time frame: Immediately before femoral arterial sheath removal, immediately after removal, and 5, 15, and 30 minutes after removal.

    Respiratory rate will be assessed by counting the participant's respirations for one minute and recorded as breaths per minute.

  7. Peripheral Oxygen Saturation

    Time frame: Immediately before femoral arterial sheath removal, immediately after removal, and 5, 15, and 30 minutes after removal.

    Peripheral oxygen saturation (SpO2) will be measured using a pulse oximeter and recorded as a percentage (%).

Study contacts

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

TUGBA ÇAM YANIK, PHD, RN

CONTACT

[email protected]

Tuğba ÇAM YANIK, PHD

CONTACT

[email protected]

05067703216

Sponsors and collaborators

Lead sponsor

Mersin University

Other

Registry information

Official study title

The Effect of Stress Ball Use During Femoral Arterial Sheath Removal After Coronary Angiography on Pain, Anxiety, Patient Satisfaction, and Hemodynamic Parameters

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Sep 9, 2026
Registry last updated
Sep 9, 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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