Trial · NCT06563570
The Effect of Teleyoga in Liver Transplant Patients
NCT06563570, Not applicable, Completed, Dokuz Eylul University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of Teleyoga in Liver Transplant Patients. Trials, record NCT06563570. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06563570
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of Teleyoga in Liver Transplant Patients
- NCT number
- NCT06563570
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 11 participants, actual
- Lead sponsor
- Dokuz Eylul University
- Conditions
- Liver Transplant Disorder
- Interventions
- yoga (online)
- First posted
- 2024-08-21
- Last updated
- 2026-05-07
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Biodex Balance System | two weeks | Balance will be assessed separately with the Biodex Balance System (Biodex Medical Systems, Inc., Shirley, NY) standing, eyes open, static and dynamic. For static and dynamic balance assessments, each test will be performed for 20 seconds with 3 repetitions. Average scores will be recorded after the evaluation. An increase in scores indicates worsening of balance and a decrease in scores indicates improvement in balance. |
| Secondary | FRAIL frailty scale | two weeks | In the FRAIL frailty scale; patients' weight loss, fatigue, slowness, decreased physical activity and weakness are examined. Those with 0 points from this questionnaire are classified as fit, those with 1-2 points are classified as pre-frail, and those with 3 or more points are classified as frail. |
| Secondary | Short Physical Performance Battery | two weeks | And The Short Physical Performance Battery consists of 3 objective tests assessing lower body function. All three physical performance measures (walking speed, balance, getting up from a chair) are scored between 0-4 according to the duration of the activity, and the scores of the three tests are summed to obtain a total score between 0 ( bad) and 12 (very good). |
| Secondary | The stroop test | two weeks | The Stroop test . On each card, there are 6 lines consisting of 4 items. These stimulus cards constitute the parts of the test and the tasks that the participant has to fulfil against these stimulus cards constitute the parts of the test. |
| Secondary | the tracking test | two weeks | There are two parts in the test, A and B. The completion time of the sequential patterns in the sections is analysed. Eight sub-scores are calculated by looking at the time, number of errors and corrections. |
| Secondary | Modified Transplantation Symptom Occurrence and Discomfort - 58-Item Scale | two weeks | Each item of the scale assesses a side effect of immunosuppressive drugs. The form assesses the frequency or intensity of symptom occurrence and the discomfort caused by the symptom in the presence of the symptom. People will be asked to tick '0' if they have not experienced any symptoms in the last 4 weeks, '1' if they have rarely, '2' if they have sometimes, '3' if they usually, or '4' if they have experienced a lot of symptoms. Afterwards, according to the distress caused by the symptom, the respondent will be asked to mark the situation he/she experienced from 0 (no distress at all) to 4 (extreme distress). |
| Secondary | short form-36 quality of life scale | two weeks | It was evaluated with Short form-36 quality of life scale. It evaluates quality of life especially in individuals with physical illness and provides measurement of quality of life in 8 dimensions: physical function (10 items), social function (2 items), role limitations due to physical problems (4 items), role limitations due to emotional problems (3 items), mental health (5 items), vitality (4 items), pain (2 items) and general perception of health (5 items). A total score is given separately for each subscale and scores range from 0-100. A score of '100' indicates good health status, while a score of '0' indicates poor health status. |
| Secondary | Beck depression scale | two weeks | Depression assessment with Beck depression scale. The scale consists of 21 items. Each item is scored between 0-3. A higher total score indicates a higher severity or level of depression. |
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.
Tests1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as |
|---|---|
| Stroop Color-Word Test | Secondary outcome |
Source ConductCognition
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/NCT06563570
GET https://conductscience.org/api/trials/v1/NCT06563570/registered