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Recruiting NCT07885449

NCT07885449 The Effect of Mind Mapping-Based Education on Postoperative Pain, Kinesiophobia, and Discharge Readiness in Patients Undergoing Total Knee Arthroplasty

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Clinical Trial Summary
NCT ID NCT07885449
Status Recruiting
Phase —
Sponsor Inonu University
Condition Total Knee Arthroplasty
Study Type INTERVENTIONAL
Enrollment 102 participants
Start Date 2026-06-01
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Mind Mapping-Based Education

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 102 participants in total. It began in 2026-06-01 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Total knee arthroplasty is a surgical procedure used to relieve pain and improve function in patients with severe knee joint problems. However, patients may experience pain, fear of movement (kinesiophobia), and difficulties in feeling ready to leave the hospital after surgery. The purpose of this study is to evaluate the effect of mind mapping-based education on postoperative pain, kinesiophobia, and discharge readiness in patients undergoing total knee arthroplasty. In this study, patients will receive education based on mind mapping in addition to routine care, or routine care alone, according to their assigned study group. Mind mapping is a visual learning method that presents information using connected words, concepts, and diagrams. The study will compare the outcomes of the groups to determine whether mind mapping-based education improves patients' postoperative experiences and readiness for discharge. Postoperative pain, fear of movement, and discharge readiness will be assessed using appropriate measurement tools. The findings may help improve patient education and support recovery after total knee arthroplasty.

Eligibility Criteria

Inclusion Criteria: * Individuals aged 18 years or older * Individuals who are literate in Turkish * Individuals without speech or hearing impairments * Individuals who are oriented to person, place, and time Exclusion Criteria: * Individuals with a neurological diagnosis (e.g., Alzheimer's disease) or a psychiatric diagnosis (e.g., schizophrenia) that may affect cognitive function * Individuals who are not literate in Turkish * Individuals undergoing bilateral total knee arthroplasty * Individuals with a history of previous orthopedic surgery

Contact & Investigator

Central Contact

Runida Doğan

✉ runida.dogan@inonu.edu.tr

📞 +90 422 377 3825

Frequently Asked Questions

Who can join the NCT07885449 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Total Knee Arthroplasty. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07885449 currently recruiting?

Yes, NCT07885449 is actively recruiting participants. Contact the research team at runida.dogan@inonu.edu.tr for enrollment information.

Where is the NCT07885449 trial being conducted?

This trial is being conducted at Batman, Turkey (Türkiye).

Who is sponsoring the NCT07885449 clinical trial?

NCT07885449 is sponsored by Inonu University. The trial plans to enroll 102 participants.

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