Pain, Postoperative Clinical Trial
Official title:
Comparison of AI-Generated Pain Scoring Visuals With Visual Analog Scale (VAS) for Pain Assessment
This prospective study will be conducted in surgical wards, assessing postoperative patients. Initially, patients will be evaluated using the VAS method. Subsequently, they will be shown five AI-generated images depicting different pain levels and will select the image that best represents their pain. A follow-up survey will assess the effectiveness of each method. Using ChatGPT-4/DALL-E, images corresponding to VAS scores of 1-2, 3-4, 5-6, 7-8, and 9-10 will be created. Patients will choose the image that best describes their pain, aiming to determine if AI-supported visuals offer a more accurate alternative to VAS for pain assessment.
Status | Not yet recruiting |
Enrollment | 398 |
Est. completion date | December 2, 2024 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years old and above - Underwent surgery for any reason - Consented to participate in the study and signed the informed consent form Exclusion Criteria: - Patients under 18 years old - Patients who did not sign the informed consent form - Patients with visual impairments - Patients whose level of consciousness is not sufficient to complete the survey - Patients with a history of psychiatric disorders |
Country | Name | City | State |
---|---|---|---|
Turkey | Health Science University Istanbul Kanuni Sultan Süleyman Education and Training Hospital | Istanbul |
Lead Sponsor | Collaborator |
---|---|
Kanuni Sultan Suleyman Training and Research Hospital |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain assesment | The primary outcome for this research is to compare the effectiveness of AI-generated pain assessment visuals with the traditional Visual Analog Scale (VAS) in accurately evaluating and expressing patients' pain levels. This will be measured through patient-reported ease of use, clarity, and usefulness of both methods, as well as patient preference for either method in pain assessment. | 10 minutes |
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