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Not Yet Recruiting NCT07900269

Effect of Stress Ball Use on Perioperative Anxiety and Postoperative Pain in Parturients Undergoing Cesarean Section

Conditions: Postoperative Pain

Sex: Female
Ages: 18 Years – 45 Years
Healthy volunteers: No
Phase: NA
Enrollment: 208
Sponsor: The Second Affiliated Hospital of Chongqing Medical University

Location: The Second Affiliated Hospital of Chongqing Medical University Chongqing China

Summary

This project aims to investigate whether the use of a stress ball during the perioperative period, as a non-invasive, drug-free, simple, and easy-to-implement intervention, can reduce the incidence of moderate-to-severe visceral pain within 24 hours after surgery in postpartum women.

Eligibility Criteria

Inclusion Criteria: 1. Scheduled for elective cesarean section under neuraxial anesthesia 2. American Society of Anesthesiologists (ASA) physical status I-III 3. Age: 18-45 years 4. Gestational age ≥ 37 weeks 5. Willing and able to understand and sign the informed consent form Exclusion Criteria: 1. Prior definite diagnosis of severe mental illness, cognitive impairment, or inability to understand pain rating scales and cooperate with the investigator; 2. Presence of preoperative chronic pain, or long-term use of analgesic drugs and psychotropic drugs (such as anxiolytics, antidepressants, etc.); 3. Hand motor dysfunction (e.g., rheumatoid arthritis)

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07900269). StuddyBuddy aggregates publicly available trial information.