Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07365761

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery

Duration - Day of surgery

Participants undergo surgery for their gynecologic cancer as part of routine care.

1 visit (in-person)

Treatment

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)

Post-operative Follow-up

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

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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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