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Total Knee ArthroplastyNCT07885449

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

A study testing Mind Mapping-Based Education in people with Total Knee Arthroplasty, run by Inonu University at 1 site in Turkey (Türkiye).

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Total Knee Arthroplasty
What is being tested?
Mind Mapping-Based Education
Could I receive a placebo?
No, everyone receives an active treatment
How many people
102 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Jun 2026to Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Individuals without speech or hearing impairments.
  • Individuals who are literate in Turkish.
  • Individuals who are oriented to person, place, and time.
  • Individuals aged 18 years or older.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Turkey (Türkiye)1 site, 1 recruiting
  • Batman Eğitim ve Araştırma Hastanesi

    Batman

    buşra Akyol, 5317994476, busragny72@gmail.com

    Buşra Akyol

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Mind Mapping-Based Education on Postoperative Pain, Kinesiophobia, and Discharge Readiness in Patients Undergoing Total Knee A

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.

Read more

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.

Read the detailed description

Mind mapping is a visual learning strategy that organizes information around a central concept through related concepts, keywords, and connections. This approach may facilitate the organization, comprehension, and recall of information by presenting complex topics in a structured visual format.

In perioperative nursing care, patients undergoing total knee arthroplasty need information about the surgical process, postoperative recovery, pain management, mobilization, and preparation for discharge. Providing structured education before and after surgery may support patients' understanding of the recovery process and encourage their active participation in postoperative care.

This randomized controlled study will investigate the effects of mind mapping-based education provided before and after total knee arthroplasty, in addition to routine care, compared with routine care alone. The intervention is designed to present perioperative information in a visual and organized format.

Participants will be randomly allocated to an intervention group or a control group. The intervention group will receive mind mapping-based education in addition to routine care, whereas the control group will receive routine care without the additional mind mapping-based educational intervention.

The study is intended to provide evidence regarding the potential contribution of mind mapping-based education to perioperative patient education and nursing care in individuals undergoing total knee arthroplasty.

Being tested
Mind Mapping-Based Education
Keywords
Total Knee Arthroplasty, Mind Mapping, Kinesiophobia, Discharge Readiness
Medical subject headings
Kinesiophobia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mind Mapping-Based EducationBehavioural

    Participants will receive mind mapping-based education before and after total knee arthroplasty, in addition to routine care. The education will cover the perioperative process, postoperative pain management, mobilization, recovery, and discharge preparation.

Study groups in NCT07885449
Study groupRoleWhat they receive
Mind Mapping-Based Education GroupExperimentalParticipants in this group will receive mind mapping-based education before and after total knee arthroplasty in addition to routine care. The education will provide structured visual information about the perioperative process, postoperative pain management, mobilization, recovery, and preparation for hospital discharge.
Receives: Behavioral: Mind Mapping-Based Education
Routine Care GroupNo interventionParticipants in this group will receive routine care, including standard patient education provided by the clinical unit, without the additional mind mapping-based educational intervention.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from Baseline in Kinesiophobia Score

    Kinesiophobia will be assessed at the initial data collection (baseline) and on postoperative day 1 using the kinesiophobia measurement instrument specified in the study protocol. The change in score from baseline to postoperative day 1 will be calculated and compared between the mind mapping-based education group and the routine care group. Scoring and interpretation will follow the instrument's guidelines.

    Measured: Baseline (initial data collection before the intervention) and postoperative day 1.

  2. Postoperative Pain Intensity on the Numeric Rating Scale

    Postoperative pain intensity will be assessed using the Numeric Rating Scale (NRS) on postoperative days 0, 1, and 2. Pain scores at each assessment time point will be compared between the mind mapping-based education group and the routine care group. Scoring will follow the version of the NRS specified in the study protocol.

    Measured: Postoperative day 0, postoperative day 1, and postoperative day 2.

  3. Readiness for Hospital Discharge Score

    Readiness for hospital discharge will be assessed using the Readiness for Hospital Discharge Scale on postoperative day 2, after the decision to discharge the patient has been made. Scores will be calculated according to the instrument's scoring guidelines and compared between the mind mapping-based education group and the routine care group

    Measured: Postoperative day 2, after the decision to discharge the patient has been made.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Oct 2026
  2. Study start1 Jun 2026
  3. Primary completionDec 2026 (estimated)
  4. Study completionDec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study uses a randomized, parallel-group, controlled experimental design. Participants will be randomly assigned to an intervention group or a control group. The intervention group will receive mind mapping-based education before and after total knee arthroplasty in addition to routine care, whereas the control group will receive routine care alone. Kinesiophobia will be assessed before the intervention and after the intervention in both groups. Postoperative pain and readiness for hospital discharge will be assessed after the intervention at the time points specified in the study protocol. Outcomes will be compared between the intervention and control groups to evaluate the effect of mind mapping-based education.
Masking
None (open label)
Enrolment
102 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07885449
Sponsor's protocol ID
2024/6360
Status last verified
Jul 2026
First submitted
14 Oct 2026
Last updated
21 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Mind Mapping-Based Education in people with Total Knee Arthroplasty, run by Inonu University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 21 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Runida Doğan (+90 422 377 3825 ext. 3846, runida.dogan@inonu.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from Baseline in Kinesiophobia Score (time frame: Baseline (initial data collection before the intervention) and postoperative day 1.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Oct 2026.

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