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Trial · NCT07887282

Registered outcomes18

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

ListOutcomeTime frameDescription
PrimaryChange in maximal inspiratory pressure (MIP)Baseline and Week 4 (end of the intervention).
Maximal inspiratory pressure (MIP) will be measured using a device with a respiratory pressure measurement function and expressed in cmH2O. Change will be calculated as the Week 4 value minus the baseline value.
PrimaryChange in Maximal Expiratory Pressure (MEP)Baseline and Week 4 (end of the intervention).
Maximal expiratory pressure was measured from total lung capacity against an occluded airway using a digital respiratory pressure meter (MicroRPM) and expressed in cmH2O. Change was calculated as Week 4 minus baseline.
SecondaryChange in forced vital capacity (FVC)Baseline and Week 4 (end of the intervention).Forced vital capacity (FVC) will be measured by spirometry and expressed in liters. Change will be calculated as the Week 4 value minus the baseline value.
SecondaryChange in Forced Expiratory Volume in 1 Second (FEV1)Baseline and Week 4 (end of the intervention).Volume exhaled in the first second of a forced exhalation maneuver was measured using spirometry, expressed in liters (L).
SecondaryChange in FEV1/FVC RatioBaseline and Week 4 (end of the intervention).The ratio of forced expiratory volume in 1 second to forced vital capacity was assessed using spirometry, expressed as a percentage (%).
SecondaryChange in Slow Vital Capacity (SVC)Baseline and Week 4 (end of the intervention).Vital capacity measured during relaxed, unforced breathing using spirometry, expressed in liters (L).
SecondaryChange in Maximal Voluntary Ventilation (MVV)Baseline and Week 4 (end of the intervention).Maximal volume of air ventilated over a 12-second sprint breathing protocol was extrapolated to liters per minute (L/min).
SecondaryChange in Seated Medicine Ball Throw DistanceBaseline and Week 4 (end of the intervention).
Upper body explosive power was measured by throwing a 3 kg medicine ball overhead from a seated position with the back supported against a wall. The maximum distance achieved across three trials was recorded in centimeters (cm).
SecondaryChange in 30-Second Modified Push-Up RepetitionsBaseline and Week 4 (end of the intervention).Upper body muscular endurance was evaluated by counting the maximum number of correctly executed push-up repetitions performed within 30 seconds.
SecondaryChange in 1-Minute Sit-Up RepetitionsBaseline and Week 4 (end of the intervention).Abdominal muscular endurance was evaluated by recording the maximum number of correctly executed sit-up repetitions completed in 60 seconds.
SecondaryChange in 1-Repetition Maximum (1RM) Bench Press StrengthBaseline and Week 4 (end of the intervention).Maximal upper body dynamic strength was assessed via 1RM barbell bench press test protocol, expressed in kilograms (kg).
SecondaryChange in 1-Repetition Maximum (1RM) Back Squat StrengthBaseline and Week 4 (end of the intervention).Maximal lower body dynamic strength was determined using a standard 1RM barbell back squat protocol, expressed in kilograms (kg).
SecondaryChange in Isometric Hand Grip StrengthBaseline and Week 4 (end of the intervention).Isometric hand grip strength was assessed using a Takei hand dynamometer for dominant and non-dominant hands, recorded in kilograms (kg).
SecondaryChange in Isometric Back and Leg StrengthBaseline and Week 4 (end of the intervention).Isometric back and leg strength were evaluated using a Takei digital back-and-leg dynamometer, recorded in kilograms (kg).
SecondaryChange in Vertical Jump HeightBaseline and Week 4 (end of the intervention).Explosive lower extremity power was evaluated via vertical jump test using a jump meter (KK 5406 Jumpmeter). The best attempt was recorded in centimeters (cm).
SecondaryChange in Single Leg Hop Performance and Limb Symmetry IndexBaseline and Week 4 (end of the intervention).
Functional lower extremity performance was measured using single-leg hop test protocols (single hop, triple hop, crossover hop, and side hop). Maximum distance was recorded in cm, and the Limb Symmetry Index (LSI, %) was calculated.
SecondaryChange in Anaerobic Peak and Mean Power (Wingate Test)Baseline and Week 4 (end of the intervention).Anaerobic power was evaluated using a 30-second all-out Wingate test on a Monark 894E cycle ergometer against a resistance of 7.5% body weight, expressed in Watts (W).
SecondaryChange in Estimated Maximal Oxygen Consumption (VO2max)Baseline and Week 4 (end of the intervention) .
Aerobic capacity was evaluated using the Bruce Treadmill Test protocol. The test began on a motorized treadmill at 2.74 km/h and a 10% incline, with speed and incline increasing every 3 minutes until volitional exhaustion. Total test duration (T, in minutes) was recorded, and VO2max was estimated using the standardized regression equation: VO2max = 14.8 - (1.379 \* T) + (0.451 \* T\^2) - (0.012 \* T\^3), expressed in mL/kg/min. Change was calculated as Week 4 minus baseline.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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