Trial · NCT07885449
The Effect of Mind Mapping-Based Education on Postoperative Pain, Kinesiophobia, and Discharge Readiness in Patients Undergoing Total Knee Arthroplasty
NCT07885449, Not applicable, Recruiting, Inonu University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of Mind Mapping-Based Education on Postoperative Pain, Kinesiophobia, and Discharge Readiness in Patients Undergoing Total Knee Arthroplasty. Trials, record NCT07885449. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07885449
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of Mind Mapping-Based Education on Postoperative Pain, Kinesiophobia, and Discharge Readiness in Patients Undergoing Total Knee Arthroplasty
- NCT number
- NCT07885449
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 102 participants, estimated
- Lead sponsor
- Inonu University
- Conditions
- Total Knee Arthroplasty
- Interventions
- Mind Mapping-Based Education
- First posted
- 2026-10-21
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change from Baseline in Kinesiophobia Score | Baseline (initial data collection before the intervention) and postoperative day 1. | 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. |
| Primary | Postoperative Pain Intensity on the Numeric Rating Scale | Postoperative day 0, postoperative day 1, and postoperative day 2. | 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. |
| Primary | Readiness for Hospital Discharge Score | Postoperative day 2, after the decision to discharge the patient has been made. | 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 |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07885449
GET https://conductscience.org/api/trials/v1/NCT07885449/registered