NCT07171957

Brief Summary

The purpose of this study was to compare the motor imagery ability of individuals with Chronic Obstructive Pulmonary Disease (COPD) with those without COPD.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
188

participants targeted

Target at P50-P75 for all trials

Timeline
8mo left

Started Aug 2025

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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 Progress54%
Aug 2025Dec 2026

Study Start

First participant enrolled

August 1, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

September 3, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

September 15, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2026

Last Updated

September 15, 2025

Status Verified

September 1, 2025

Enrollment Period

1.2 years

First QC Date

September 3, 2025

Last Update Submit

September 10, 2025

Conditions

Keywords

mental imageryChronic Obstructive Pulmonary Disease

Outcome Measures

Primary Outcomes (1)

  • Kinesthetic and Visual Motor Imagery Questionnaire-20 (KVIQ-20)

    Developed to assess imagery ability, the questionnaire aims to determine the extent to which individuals visualize and feel the movements they imagine. The KVIQ-20 consists of 10 visual and 10 kinesthetic items that assess head, shoulders, trunk, upper extremity, and lower extremity movements. All 10 movements are performed in a sitting position. The KVIQ uses a 5-point scale to rate the clarity of imagery (Visual subscale) and the intensity of sensations (Kinesthetic subscale); a score of 5 corresponds to the highest level of imagery and a score of 1 corresponds to the lowest level of imagery. During the test, bilateral assessments are performed. A validity and reliability study for the Turkish version was conducted by Dilek and colleagues. Individuals will be instructed to use a first-person perspective during the MI.

    Baseline (First assessment)

Secondary Outcomes (2)

  • Mental Chronometry Test

    Baseline (First assessment)

  • Mental Rotation Test

    Baseline (First assessment)

Other Outcomes (1)

  • Edinburgh Handedness Questionnaire

    Baseline (First assessment)

Study Arms (2)

COPD group

Study group

Control Group

Healthy group

Eligibility Criteria

Age40 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Chest diseases clinic

You may qualify if:

  • Being between 40-70 years of age
  • Being diagnosed with COPD
  • Having 24 points or more on the Mini Mental State Examination
  • Not having a history of acute exacerbation and/or hospitalization in the last month and being clinically stable

You may not qualify if:

  • Being between 40-70 years old
  • Having a score of 24 or above on the Mini Mental State Examination
  • Not having any pulmonary, cardiac, orthopedic or neurological disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kütahya Health Sciences University

Kütahya, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Lütfiye AKKURT, Asst.Prof.

    Kütahya Health Sciences University

    STUDY DIRECTOR
  • İlknur KAYA, Asst.Prof.

    Kütahya Health Sciences University

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 3, 2025

First Posted

September 15, 2025

Study Start

August 1, 2025

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

December 30, 2026

Last Updated

September 15, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations