NCT07805304

Brief Summary

This study assess the efficacy of digital avatar-assisted pre- and post-operative information against nurse-led oral and written information following SRM3 including an analysis of potential risk factors associated with impaired convalescent

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2025

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

August 24, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 24, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

September 4, 2026

Completed
Last Updated

September 4, 2026

Status Verified

September 1, 2026

Enrollment Period

8 months

First QC Date

August 24, 2026

Last Update Submit

September 3, 2026

Conditions

Keywords

Dentistry, Embodied Conversational Agent, Patient-reported outcome measures, Surgery, Surveys and questionnaires, Third molar

Outcome Measures

Primary Outcomes (2)

  • Confidence with the pre- and post-operative information

    Confidence with the pre- and post-operative information following surgical removal of an mandibular third molar was assessed by a 7-item questionnaire. Response format was yes/no or by visuel analoque scale (0 = not satisfied to 100 = extremely satisfied).

    1. prior to surgical removal of a mandibular third molar

  • Confidence with the pre- and post-operative information

    Confidence with the pre- and post-operative information with the pre- and postoperative information will be assessed by validated questionnaire

    Confidence with the pre- and post-operative information will be assessed prior to and immediately after surgical removal of an mandibular third molar

Study Arms (1)

Avatar-assisted pre- and post-operative information

EXPERIMENTAL

Pre- and postoperative information is provided by an avatar following surgical removal of mandibular third molar

Procedure: Avatar-assisted pre- and post-operative information following surgical removal of an mandibular third molar

Interventions

Standardized pre- and postoperative information will be provided by Avatar-assisted or nurse-led following surgical removal of an mandibular third molar

Also known as: Nurse-led pre- and postoperative information following surgical removal of an mandibular third molar
Avatar-assisted pre- and post-operative information

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • A partially or totally impacted mandibular third molar.
  • Indication for surgical removal of a mandibular third molar.
  • Age between 18-80.

You may not qualify if:

  • Previous surgical removal of mandibular third molar.
  • Indication for other surgical interventions within the oral cavity including upper third molar removal in conjunction with surgical removal of mandibular third molar.
  • Infection and inflammatory symptoms in the oral cavity at the time of surgical removal of mandibular third molar.
  • Medication with antiresorptive agents or daily analgesics.
  • ASA score 3 or above.
  • Reduced bone healing capacity due to severe anemia, hypothyroidism, or poor nutrition.
  • Previous radiotherapy for head and neck cancer.
  • Psychological disease.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Oral and Maxillofacial Surgery, Aalborg University Hospital

Aalborg, North Denmark, 9000, Denmark

Location

Related Publications (1)

  • Author

    RESULT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Model Details: A randomized controlled trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

August 24, 2026

First Posted

September 4, 2026

Study Start

October 1, 2024

Primary Completion

May 30, 2025

Study Completion

August 24, 2026

Last Updated

September 4, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

Locations