Actively Recruiting
Emotional Assessment and Tiered Individualized Psychological Support for Newly Diagnosed Postoperative Gynecologic Patients Using the E-MOTE Artificial Intelligence Robot
Led by National Taiwan University Hospital · Updated on 2026-01-26
130
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are developing the E-MOTE robot, designed to help newly diagnosed gynecological cancer patients manage their emotions during the surgical treatment process. This study, based on the Social Cognitive Theory of Self-Regulation, aims to evaluate the robot's effectiveness in reducing psychological distress, physical symptoms, stress levels, and improving quality of life. The research also includes interviews with nursing staff to gather their views on the robot's clinical use. Participants will be randomly assigned to either routine care or the intervention group receiving the E-MOTE robot. Those in the intervention group will interact with the robot on the first and second days after surgery, which performs emotional assessments, tailored dialogue based on distress levels, empathetic conversations, a session of self-affirmation relaxation training, and a Q&A session. The study involves wearing a smart wearable device, and both groups complete pre- and post-test questionnaires. Participants will be evaluated before the intervention, three days after surgery, and one week after discharge through measures including distress, depression, quality of life, loneliness, symptom severity, and physiological indicators. Usability of the robot will be assessed three days post-surgery. The study monitors emotional and physical outcomes during and after the surgical treatment period, with the total involvement lasting up to one week after discharge.
CONDITIONS
Brief Title
Emotional Assessment and Tiered Individualized Psychological Support of the Artificial Intelligence Robot
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years or older
- Diagnosed with gynecologic cancer and undergoing or scheduled for surgery
- Willing to receive the E-MOTE robot support and wear a smart wearable device
- Willing to complete pre-test and post-test questionnaires
- Clinical nurses aged 18 or older who have cared for patients receiving the E-MOTE robot (for nursing staff participation)
You will not qualify if you...
- Unable to communicate clearly
- Unwilling or unable to participate in the study in its entirety
- Nurses unwilling to take part in qualitative interviews
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo surgery for their gynecologic cancer as part of routine care.
1 visit (in-person)
Duration - 2 days after surgery
Participants in the intervention group receive the E-MOTE robot intervention on the first and second days after surgery, including emotional assessments, tailored dialogue modules, self-affirmation relaxation training, and a Q&A session.
2 visits (in-person or bedside)
Duration - From pre-intervention through one week after discharge
Participants complete follow-up assessments measuring distress, depression, quality of life, loneliness, symptom severity, and physiological indicators before the intervention, three days after surgery, and one week after discharge.
3 visits (in-person or remote assessments)
Trial Site Locations
Total: 1 location
1
National Taiwan University
Taipei, Taiwan
Actively Recruiting
Research Team
Y
Yun-Hsiang Lee Associate Professor, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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