Effect Of Resistance Training On Physical Fitness, Cognitive Ability, And Academic Performance In Young Adults
NCT06086808, Not applicable, Unknown, Riphah International University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effect Of Resistance Training On Physical Fitness, Cognitive Ability, And Academic Performance In Young Adults | ClinicalTrials.gov |
| NCT number | NCT06086808 | ClinicalTrials.gov |
| Status | Unknown | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 20 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Riphah International University | ClinicalTrials.gov |
| Conditions | Young Adults | ClinicalTrials.gov |
| Interventions | Resistance Training, General Fitness and Toning | ClinicalTrials.gov |
| First posted | 2023-10-17 | ClinicalTrials.gov |
| Last updated | 2023-10-17 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Isometric Strength (lbs) | Baseline and after end of the intervention (3 months) | Isometric Strength will be assessed using a Hand-held Dynamometer measuring isometric contraction force in pounds (lbs). | ClinicalTrials.gov |
| Primary | Endurance | Baseline and after end of the intervention (3 months) | Endurance will be assessed using the Yo Yo Intermittent Recovery Level 1 Test ranging from speed level 5 (lightest) to speed level 23 (hardest). | ClinicalTrials.gov |
| Primary | Agility | Baseline and after end of the intervention (3 months) | Agility will be assessed using Illinois Agility Run Test (Time to complete it in seconds). | ClinicalTrials.gov |
| Primary | Balance | Baseline and after end of the intervention (3 months) | Balance will be assessed using Star Excursion Balance Test (distance in each direction). | ClinicalTrials.gov |
| Primary | Stroop Test | Baseline and after end of the intervention (3 months) | Stroop test will be used to assess cognitive function (number of items completed during each task). | ClinicalTrials.gov |
| Primary | Trail Making Test | Baseline and after end of the intervention (3 months) | Trail Making Test will be used to assess cognitive function (time spent to complete the task). | ClinicalTrials.gov |
| Primary | Verbal Digit Span Test | Baseline and after end of the intervention (3 months) | Verbal Digit Span Test will be used to assess cognitive function (number of digits recalled correctly). | ClinicalTrials.gov |
| Primary | Academic Performance | Baseline and after end of the intervention (3 months) | Academic performance will be assessed using previous and subsequent school grades of the participants. | 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 4
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 |
|---|---|---|
| Digit Span Test | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
| Trail Making Test A | Primary outcome | ConductCognition |
| Trail Making Test B | Primary 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)