Clinical trial · Interventional
Emotional Assessment and Tiered Individualized Psychological Support of the Artificial Intelligence Robot
Emotional Assessment and Tiered Individualized Psychological Support for Newly Diagnosed Postoperative Gynecologic Patients: Development and Testing of the E-MOTE Artificial Intelligence Robot
NCT07365761CI-TRIAL-00101633recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To develop the E-MOTE robot and evaluate its effectiveness in addressing psychological distress, physical symptom, stress index, and quality of life, as well as to explore its clinical applicability.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Emotional Assessment | — | UNRESOLVED | — |
| Gynecological Cancers | — | UNRESOLVED | — |
| Nursing | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| E-MOTE group | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- NO_INTERVENTION
- label
- Control Group
- description
- Routine care
- type
- EXPERIMENTAL
- label
- Intervention Group
- description
- The intervention group will receive the E-MOTE robot, which conducts emotional assessments, and provides a session of self-affirmation relaxation training followed by a Q\&A session.
- interventionNames
- Other: E-MOTE group
Primary outcomes (2)
- measure
- Distress
- timeFrame
- Measurements will be taken before the intervention, three days after surgery, and one week after discharge.
- description
- Investigators utilized the Distress Thermometer(DT) as the primary outcome measure. The scale uses a 11 Liker scale, where 0 indicates no distress at all and 10 represents the most severe distress.Higher score indicates a more severe distress. When the score is 4 or higher, a Problem List (PL) is used to further identify factors contributing to the emotional distress.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Stage 1 (For patients and nurse) \*\*\*Patients\*\*\* Inclusion Criteria: * Aged 18 years or older. * Diagnosed with gynecologic cancer and undergoing surgery. * Willing to receive E-MOTE robot and wear a smart wearable device. * Willing to complete pre-test and post-test questionnaires. Exclusion Criteria: * Unable to communicate clearly. * Unwilling or unable to participate in the study in its entirety. \*\*\*Nurse\*\*\* Inclusion Criteria: * Aged 18 years or older. * As a clinical nurse and has cared for patients who received the E-MOTE robot Exclusion Criteria: \- Unwilling to participate in the qualitative interview. Stage 2 (only for patients) \*\*\*Intervention group\*\*\* Inclusion Criteria: * Aged 18 years or older. * Diagnosed with gynecologic cancer and scheduled to undergo surgery. * Willing to receiveE-MOTE robot and to wear a smart wearable device. * Willing to complete pre-test and post-test questionnaires. Exclusion Criteria: * Unable to communicate clearly. * Unwilling or unable to participate in the study in its entirety. \*\*\*Control group\*\*\* Inclusion Criteria: * Aged 18 years or older. * Diagnosed with gynecologic cancer and scheduled to undergo surgery. * Willing to complete pre-test and post-test questionnaires. Exclusion Criteria: * Unable to communicate clearly. * Unwilling or unable to participate in the study in its entirety.
References
Publications (0)
Data not yet available
No reference posted for this study.