NCT07202286

Brief Summary

This study aimed to compare the patient acceptability (preference, length, and difficulty) and accuracy of Chat-Generative Pre-Trained Transformer (ChatGPT) responses to questions from people with osteoarthritis (OA) with physician responses.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
286

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2024

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

May 22, 2024

Completed
14 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 5, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 5, 2024

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

September 30, 2025

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 1, 2025

Completed
Last Updated

October 6, 2025

Status Verified

October 1, 2025

Enrollment Period

14 days

First QC Date

September 30, 2025

Last Update Submit

October 1, 2025

Conditions

Keywords

chatGPTOsteoarthritisAcceptabilityAccuracyArtificial IntelligenceCross-sectional

Outcome Measures

Primary Outcomes (1)

  • Preferred response

    Binary outcome, chatbot or physician response. This was an average based on the preferences on the 7 FAQs.

    From invitation until the end of the study at two weeks

Secondary Outcomes (3)

  • Rating of length

    From invitation until the end of the study at two weeks

  • Rating of difficulty

    From invitation until the end of the study at two weeks

  • Accuracy

    From invitation until the end of the study at two weeks

Other Outcomes (1)

  • Number of words of the responses

    This was determined before the study started

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

There were two groups of participants: 1) a panel of people with OA evaluating the preference, length, and difficulty, and 2) a panel of experts in the field of OA evaluating the accuracy of the responses

You may qualify if:

  • all individuals visiting the Department of Orthopedics in the Canisius Wilhelmina Hospital, a district general hospital in Nijmegen, The Netherlands, diagnosed with knee or hip OA between March 2023 and March 2024

You may not qualify if:

  • partly completion of the questionnaire

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Canisius Wilhelmina Hospital

Nijmegen, Netherlands

Location

MeSH Terms

Conditions

Osteoarthritis

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 30, 2025

First Posted

October 1, 2025

Study Start

May 22, 2024

Primary Completion

June 5, 2024

Study Completion

June 5, 2024

Last Updated

October 6, 2025

Record last verified: 2025-10

Locations