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Manual Lymphatic Drainage Versus Classical Massage on Heart Responses and Mood in Hemodialysis

NCT07932483, Not applicable, Not yet recruiting, Mersin University

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleManual Lymphatic Drainage Versus Classical Massage on Heart Responses and Mood in HemodialysisClinicalTrials.gov
NCT numberNCT07932483ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment60 participants, estimatedClinicalTrials.gov
Lead sponsorMersin UniversityClinicalTrials.gov
ConditionsRenal Dialysis, Renal Insufficiency, Chronic, Manual Lymphatic Drainage, Massage, Affect (Mental Function)ClinicalTrials.gov
InterventionsManual Lymphatic Drainage, Classical MassageClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryStandard Deviation of Normal-to-Normal Intervals (SDNN)Before the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
PrimaryRoot Mean Square of Successive Differences (RMSSD)Before the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
PrimaryLow Frequency (LF) PowerBefore the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
PrimaryHigh Frequency (HF) PowerBefore the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
PrimaryLow Frequency to High Frequency Ratio (LF/HF)Before the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
PrimarySystolic Blood PressureBefore the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
PrimaryDiastolic Blood PressureBefore the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
PrimaryHeart RateBefore the intervention, immediately after the 20-minute intervention, and 30 minutes after the post-intervention measurement, in each periodClinicalTrials.gov
SecondaryFatigue Subscale Score of the Profile of Mood States - Short FormBefore and immediately after the 20-minute intervention, in each intervention periodClinicalTrials.gov
SecondaryVigor Subscale Score of the Profile of Mood States - Short FormBefore and immediately after the 20-minute intervention, in each intervention periodClinicalTrials.gov
SecondaryTension Subscale Score of the Profile of Mood States - Short FormBefore and immediately after the 20-minute intervention, in each intervention periodClinicalTrials.gov
SecondaryConfusion Subscale Score of the Profile of Mood States - Short FormBefore and immediately after the 20-minute intervention, in each intervention periodClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)