NCT07102420

Brief Summary

The aim of this study is to compare artificial intelligence anxiety (AIA) in athletes and sedentary individuals, evaluate its relationship with exercise frequency, and identify the subdimensions that cause high anxiety at the level of AIA scale items.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
663

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2025

Shorter than P25 for all trials

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

First Submitted

Initial submission to the registry

July 28, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 3, 2025

Completed
17 days until next milestone

Study Start

First participant enrolled

August 20, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 20, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 20, 2025

Completed
Last Updated

February 4, 2026

Status Verified

July 1, 2025

Enrollment Period

1 month

First QC Date

July 28, 2025

Last Update Submit

February 2, 2026

Conditions

Keywords

physical activityartificial intelligence anxietyathletes

Outcome Measures

Primary Outcomes (1)

  • Artificial Intelligence Anxiety Scale

    The Artificial Intelligence Anxiety Scale (AIAS) is an assessment tool that asks each participant to reflect on their current experiences. It is a 7-point Likert-type scale, ranging from 1 (not at all) to 7 (completely). The scale consists of four subdimensions: learning, job replacement, socio-technical blindness, and AI configuration. The total score ranges from a minimum of 21 to a maximum of 147. Higher scores indicate higher levels of anxiety experienced in relation to artificial intelligence.

    baseline

Study Arms (2)

Sedentary individuals

Sedentary individuals who have not engaged in regular exercise within the past six months, who have been exposed to basic concepts of artificial intelligence (through media, news, education, etc.), who possess sufficient cognitive ability to complete the questionnaires, and who do not have any chronic neurological, orthopedic, cardiovascular, or psychological conditions.

Other: Questionnaire and Physical Exam

Athletes

Licensed athletes who have engaged in regular exercise or sports at least twice a week during the past six months, who have been exposed to basic concepts of artificial intelligence (through media, news, education, etc.), who possess sufficient cognitive capacity to complete the questionnaires, and who do not have any chronic neurological, orthopedic, cardiovascular, or psychological conditions.

Other: Questionnaire and Physical Exam

Interventions

Artificial Intelligence Anxiety Scale

AthletesSedentary individuals

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

The study plans to include healthy individuals aged 18 to 45 years, consisting of both regularly exercising participants and sedentary individuals.

You may qualify if:

  • Being between 18 and 45 years of age
  • Having engaged in regular exercise or sports at least twice a week over the past six months (for athlete group)
  • Not having engaged in regular exercise during the past six months (for sedentary group)
  • Being exposed to basic concepts of artificial intelligence (via media, news, education, etc.)
  • Having sufficient cognitive ability to complete the questionnaires

You may not qualify if:

  • Having a chronic neurological, orthopedic, cardiovascular, psychological, or similar medical condition
  • Having a serious physical disability that prevents participation in exercise
  • Incomplete or inconsistent responses in the questionnaires
  • Having undergone a recent surgical operation
  • Lack of voluntary consent to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kto Karatay University

Konya, Karatay, 42030, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor Activity

Interventions

Surveys and QuestionnairesRestraint, Physical

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public HealthBehavior ControlTherapeuticsImmobilization

Study Officials

  • Özlem Akkoyun Sert, PhD

    KTO Karatay University

    STUDY CHAIR
  • Fatma Çiftçi, PhD

    KTO Karatay University

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 28, 2025

First Posted

August 3, 2025

Study Start

August 20, 2025

Primary Completion

September 20, 2025

Study Completion

October 20, 2025

Last Updated

February 4, 2026

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations