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Effect of Perioperative Use of a Stress Relief Ball on Anxiety and Pain in Adult Patients Undergoing Strabismus Surgery under Local Anesthesia

Effect of Perioperative Use of a Stress Relief Ball on Anxiety and Pain in Adult Patients Undergoing Strabismus Surgery under Local Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126068
Enrollment
Unknown
Registered
2026-06-03
Start date
2026-06-03
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Strabismus

Interventions

Decompression ball group:Use of a silicone decompression ball with a diameter of approximately 5cm and medium hardness. Thirty minutes before surgery, the research nurse provides the decompression bal
Routine care group:Receive the same perioperative nursing procedures, but no decompression ball is provided. Control group patients rest quietly and receive surgery during the same time period.

Sponsors

Qingdao Eye Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-65 years old; 2. American Society of Anesthesiologists (ASA) Grade I-II; 3. Strabismus correction surgery will be performed under local anesthesia at an appropriate time; 4. The estimated operation time is <=30 minutes; 5. Be conscious and capable of reading, understanding and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Presence of severe visual, auditory, or cognitive impairment that hinders effective communication or use of a stress relief ball. 2.History of major psychiatric disorders or long-term use of anxiolytic/antidepressant medications. 3.Presence of severe or uncontrolled systemic comorbidities that may significantly affect perioperative stress response, pain perception, or emotional regulation. 4.Conversion to general anesthesia during surgery; 5.Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
Intraoperative Anxiety Level;

Secondary

MeasureTime frame
Assess hemodynamic stability;Postoperative Satisfaction;Intraoperative Pain Level;

Countries

China

Contacts

Public ContactSun Xiaolin

Qingdao Eye Hospital of Shandong First Medical University

xiaolinsunny@126.com+86 532 85883079

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026