← Back to all trials
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)
Source: ClinicalTrials.gov (NCT07900269). StuddyBuddy aggregates publicly available trial information.