Diaphragmatic and Box Breathing on Heart Rate Variability and Perceived Stress
NCT07698652, Not applicable, Recruiting, Cairo University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Diaphragmatic and Box Breathing on Heart Rate Variability and Perceived Stress | ClinicalTrials.gov |
| NCT number | NCT07698652 | ClinicalTrials.gov |
| Status | Recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 60 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Cairo University | ClinicalTrials.gov |
| Conditions | Stress, Psychological Resilience, Healthy Students | ClinicalTrials.gov |
| Interventions | Diaphramatic Breathing Training, Box Breathing Training | ClinicalTrials.gov |
| First posted | 2026-07-13 | ClinicalTrials.gov |
| Last updated | 2026-09-28 | ClinicalTrials.gov |
Registered outcomes 5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Heart Rate Variability | Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention). | HRV will be measured using the Polar H10 sensor and analyzed through Kubios HRV software to evaluate physiological resilience and autonomic nervous system regulation. | ClinicalTrials.gov |
| Primary | Perceived Stress | Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention). | Stress will be measured using the Perceived Stress Scale (PSS-10). The total score ranges from a minimum of 0 to a maximum of 40. Higher scores indicate higher levels of perceived stress, representing a worse outcome | ClinicalTrials.gov |
| Primary | Resilience | Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention). | Resilience will be measured using the Brief Resilience Scale (BRS). The score ranges from a minimum of 1 to a maximum of 5. Higher scores indicate higher levels of resilience, representing a better outcome | ClinicalTrials.gov |
| Secondary | Cognitive Performance | Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention). | Cognitive performance will be assessed using the Stroop Color-Word Test. The score represents the number of correct responses. The minimum possible score is 0, with no strictly defined maximum. Higher scores indicate better cognitive performance, representing a better outcome | ClinicalTrials.gov |
| Secondary | Academic Achievement | Baseline (pre-intervention) and at the end of the 4-week training period (post-intervention). | Academic achievement will be assessed using the 9-item Academic Self-Efficacy Scale (ASE). The total score ranges from a minimum of 9 to a maximum of 63. Higher scores indicate higher levels of academic self-efficacy, representing a better outcome | 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 1
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 |
|---|---|---|
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
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)