Impacts of Concurrent Training on Heart Rate Variability, Hemodynamic Parameters, and Behavioral Aspects of Older Adults
NCT07925905, Not applicable, Completed, Universidade do Estado do Pará
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Impacts of Concurrent Training on Heart Rate Variability, Hemodynamic Parameters, and Behavioral Aspects of Older Adults | ClinicalTrials.gov |
| NCT number | NCT07925905 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 44 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Universidade do Estado do Pará | ClinicalTrials.gov |
| Conditions | Older Adults (60 - 85 Years Old) | ClinicalTrials.gov |
| Interventions | concurrent training intervention, endurance training intervention, resistance training intervention | ClinicalTrials.gov |
| First posted | 2026-11-09 | ClinicalTrials.gov |
| Last updated | 2026-11-09 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | heart rate variability | 12 weeks | MeanNN | ClinicalTrials.gov |
| Primary | heart rate variability | 12 WEEKS | SDNN | ClinicalTrials.gov |
| Primary | Heart rate variability | 12 WEEKS | RMSSD | ClinicalTrials.gov |
| Primary | Heart rate variability | 12 WEEKS | high frequency band (HF) | ClinicalTrials.gov |
| Secondary | Systemic blood pressure, heart rate and double product | 12 WEEKS | systolic blood pressure, diastolic blood pressure and heart rate (bpm) | ClinicalTrials.gov |
| Secondary | sleep quality | 12 weeks | PSQI (pittsburgh sleeping quality index). Sleep quality was assessed using the Pittsburgh Sleep Quality Index (PSQI), with a global score ranging from 0 to 21 points, where higher scores indicate poorer sleep quality. Scores greater than 5 are conventionally used to identify individuals with poor sleep quality (Buysse et al., 1989). | ClinicalTrials.gov |
| Secondary | BMI | 12 weeks | Kg/m2 | ClinicalTrials.gov |
| Secondary | perceived stress | 12 WEEKS | using EPS-10 scale. Perceived stress was assessed using the 10-item Perceived Stress Scale (PSS-10), with a total score ranging from 0 to 40 points, where higher scores indicate greater levels of perceived stress (Cohen et al., 1983). | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
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 | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
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)