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Recruiting NCT07108192

The Effect of Hand Holding and Stress Ball Intervention on Pain and Anxiety

No phase Interventional Cataract Surgery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Hand Holding, Stress Ball, Control Group.
Who it may be relevant to
Registry conditions: Cataract Surgery. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Hand Holding and Stress Ball Intervention on Pain and Anxiety During Cataract Surgery: A Randomized Controlled Trial

Overview

Cataract surgery is currently primarily performed with topical anesthesia. Although topical anesthesia provides many benefits for patients, they may experience pain, anxiety and discomfort during surgery. It has been reported that increased pain and anxiety during surgery may decrease patient cooperation and satisfaction, making surgery more difficult. In this context, in addition to medical interventions, non-pharmacologic methods are recommended to manage pain and anxiety during surgery. Non-pharmacological methods are reported to be simple, effective and cost-effective. In this context, studies have shown that stress ball application and hand holding are effective strategies for the control of pain and anxiety in patients. According to this information, the aim of this study was to evaluate the effect of stress ball application and hand holding method used during cataract surgery on patients' pain and anxiety. Another aim of the study was to determine the effects of stress ball application and hand holding method on patients' satisfaction levels and vital signs.

Detailed description

Cataract is the main cause of visual impairment and blindness globally and surgery remains the only effective treatment for cataract. Today, it is a common procedure for routine cataract surgery under topical anesthesia. Topical anesthesia is most commonly used because it eliminates potential complications such as optic nerve damage, retrobulbar hemorrhage and ocular muscle injury. However, topical anesthesia does not eliminate pain sensitivity of the iris, zonule and ciliary body during cataract surgery. Moreover, patients may experience discomfort due to manipulation of intraocular structures during surgery. However, patients are awake during surgery to follow the surgeon's instructions, which can lead to anxiety and adverse consequences in physiologic parameters such as tachycardia and hypertension. Patients may move during surgery due to anxiety and pain, and may lose visual function due to bleeding or post-surgical complications such as glaucoma. Therefore, assessing and controlling pain and anxiety during surgery is important for patient comfort and surgical prognosis. Moreover, the management of pain and anxiety during surgery not only reduces patients' anxiety but also increases patient cooperation during surgery. In this context, pharmacological as well as non-pharmacological methods are widely used in the management of pain and anxiety. Although the effects of hand holding and stress ball application on patients' pain, anxiety, satisfaction levels and vital signs in various contexts have been reported, their effects, especially during cataract surgery, have not been sufficiently investigated. Therefore, this study aims to contribute to the existing literature by examining the effects of hand holding and stress ball application on patients' pain, anxiety, satisfaction levels and vital signs during cataract and to provide evidence for the importance of the use of nonpharmacologic methods.

Interventions

  • Other Hand Holding
    Hand holding intervention will be performed by the researcher. Before cataract surgery, the researcher will sit in a chair next to the patient and warm his/her hands to a level that does not disturb the patient. 1-2 minutes before cataract surgery, the researcher will hold the patient's hand without gloves, with one hand, with moderate pressure, without rubbing or squeezing it uncomfortably. The hand holding intervention will continue until the cataract surgery is completed
  • Other Stress Ball
    According to the randomization, the patient in the stress ball group will first be taught the use of stress balls face to face by the researcher. The researcher will place a round, medium-hard, high-quality stress ball of the same brand in the patient's active hand 1-2 minutes before the cataract surgery is started. The patient will be asked to squeeze and relax the stress ball by counting to 5 during cataract surgery. After squeezing the stress ball, he/she should count to 5 and then loosen it.
  • Other Control Group
    Patients who did not receive any intervention other than standard treatment and care during cataract surgery were defined as the control group.

Primary outcome measures

  • Anxiety levels [Time frame: Anxiety levels of the patients will be evaluated in 2 stages, 15 minutes before surgery and 15 minutes after the surgery is completed.]
  • Pain levels [Time frame: Patients' pain levels will be evaluated in 2 stages: intraoperatively and 15 minutes after the operation is completed]
Secondary outcome measures (5)
  • Patient satisfaction level [Time frame: Patients' satisfaction levels will be assessed in a single stage 15 minutes after the operation is completed]
  • Physiological parameters-blood pressure [Time frame: Patients' blood pressure will be measured 15 minutes before surgery and 15 minutes after surgery is completed.]
  • Physiological parameters-pulse rate [Time frame: The pulse rate of the patients will be measured 15 minutes before surgery and 15 minutes after surgery is completed.]
  • Physiological parameters-respiratory rate [Time frame: The respiratory rate of the patients will be measured 15 minutes before surgery and 15 minutes after surgery is completed.]
  • Physiological parameters-oxygen saturation [Time frame: Oxygen saturation of the patients will be measured 15 minutes before surgery and 15 minutes after surgery is completed.]

Eligibility criteria

Inclusion criteria

  • 18 years and over
  • Can understand and speak Turkish
  • Clear consciousness, person, place and time oriented
  • No hearing and perception problems
  • Does not have any mental or neurological disorders that may affect communication (Alzheimer's, dementia, etc.)
  • First time cataract surgery
  • Those without any psychiatric diagnosis/ treatment (antidepressants, anxiolytics, sedatives, etc.)
  • No physical problems in squeezing the stress ball (muscle, joint problems, etc.)
  • No analgesic or anesthetic medication 24 hours before the procedure
  • Individuals who agree to participate in the study will be included in the study

Exclusion criteria

  • Conversion of topical anesthesia to general anesthesia during surgery
  • A different story of eye surgery
  • Hearing, speech, physical or mental disability
  • Pregnancy or possible pregnancy
  • Those with malignancy
  • Taking an analgesic medication at least 24 hours before the procedure
  • People with chronic pain
  • History of incomplete or canceled cataract procedures
  • Hypertension in the patient (>160/100 mmHg)
  • Suppurative/infective/inflammatory skin condition of the hands
  • Hypersensitivity to touch
  • Patients with contact-transmitted diseases
  • Being uncomfortable with hand-holding,
  • In case of need for emergency intervention by a physician during or immediately after the procedure
  • Failure to perform the stress ball application in accordance with the instruction
  • Pre-existing neuropathy (muscle joint problem, stroke, etc.)
  • Complications during cataract surgery
  • Those who want to leave the study voluntarily
  • Termination of the procedure due to deterioration of the patient's general condition during the procedure
  • Failure to carry out intervention practices in accordance with the determined protocol (Dropping the stress ball during the procedure, etc.)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • Yenikent State Hospital — Sakarya

Identifiers

NCT: NCT07108192 · E-43012747-050.04-489789-435

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗