Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06232343
Other study ID # REC/RCR&AHS/23/0760
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 1, 2023
Est. completion date February 5, 2024

Study information

Verified date January 2024
Source Riphah International University
Contact Imran amjad, PhD
Phone 9233224390125
Email imran.amjad@riphah.edu.pk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Muscular power may protect against cardiovascular disease independently of cardiorespiratory fitness. Resistance training is a useful training technique to boost running speed while enhancing other aspect of an athlete's physical condition. Resistance training is also consisting of weight training. Weight training emphasis on health exercise program. Improvements in muscular strength, power, running speed, kicking velocity, endurance, dynamic balance, flexibility, and general motor function have been observed in youth who have participated in resistance training between the ages of 8 to 14 years. These improvements strengthen young athletes' immunity to common sports ailments It will be Randomized Controlled trial in which convenient sampling technique will be used. Two groups will be formed in which participants will be divided by lottery method. Group A in which will be treated By Parachute resistance training and the other group will perform sprinters. Fatigue Assessment Scale and Strength 1RM tool will be used. The result after statistical analysis will either show this intervention is effective or not. Results will be analyzed on SPSS


Description:

The study plan consisted of three parts, a) initial evaluation testing b) implementation of a 4-week intervention training programme c) evaluation retesting. The resisted sprint training method will be adopted. To achieve resistance, a parachute will be used. The rate of applied resistance should be such that no alteration of the running technique would be observed. Any running velocity decrease 10% compared to un-resisted running indicates that the applied resistance load is too high and will have adverse effects on the sprinting technique. The subjects will be divided randomly into two groups (Ν = 21each). Both groups will follow the same training programmed. The first group followed a resisted training programmed with a parachute (resisted group-RG), while the other group used no external resistance (un-resisted group-UG).control group perform sprinters. The training programmed will have duration of four weeks and will be implemented in the same facility in which the evaluation procedures will be held. The preparation/warm-up protocol throughout the training programmed will be the same with the protocol that was implemented during the testing procedures. The groups will follow the training programmed three times a week. The daily schedule (training group) included four repetitions of maximum intensity 30 m & 50 m dashes (4 × 30 m, 4 × 50 m). The duration of recovery time between the 30 m & 50 m runs will be 4 and 6 minutes respectively. Between the last 30 m dash and the first 50 m dash, a 10-minute recovery will be applied. With regard to the frequency and volume of the intervention programmed, sprint - speed training is characterized by maximum intensity stimuli to be repeated 2-4 times a week. Moreover, sprint - speed training should not exceed 400-500 meters in total . To this end, the training programmed of the present study consisted of 4x30m and 4x50m runs, at a frequency of 3 times a week. (Total volume = 120 m + 200 m = 320 m). The duration of the recovery time will be 4 and 6 minutes for the 30 m and 50 m runs respectively, and 10 minutes between each set. 4-minutes of recovery time is adequate for the body to reach full recovery. A recovery time longer than 12 minutes between repetitions in total results in inactivation of the central nervous system


Recruitment information / eligibility

Status Recruiting
Enrollment 42
Est. completion date February 5, 2024
Est. primary completion date February 5, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 14 Years
Eligibility Inclusion Criteria: - Age 08-14 years - Athletic Participants will be included - Both Gender Boys and Girls will be included Exclusion Criteria: - Participants with any musculoskeletal, neurological, cardiovascular, or respiratory disablements - Those who were unable to complete follow-up tests. - Participants with leg length discrepancy. - Participants Previous surgery - Participants are not currently using or ever used supplements that can effect muscles

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Parachute Resistance Training
The training programmed duration is of four weeks.The groups will follow the training programmed three times a week. The daily schedule (training group) included four repetitions of maximum intensity 30 m & 50 m dashes (4 × 30 m, 4 × 50 m). The duration of recovery time between the 30 m & 50 m runs will be 4 and 6 minutes respectively. Between the last 30 m dash and the first 50 m dash, a 10-minute recovery will be applied. Moreover, sprint speed training should not exceed 400-500 meters in total . To this end, the training programmed of the present study consisted of 4x30m and 4x50m runs, at a frequency of 3 times a week.
Sprinters
control group perform sprinters without any external resistance training for four weeks.

Locations

Country Name City State
Pakistan Riphah International University Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

References & Publications (2)

Walters BK, Read CR, Estes AR. The effects of resistance training, overtraining, and early specialization on youth athlete injury and development. J Sports Med Phys Fitness. 2018 Sep;58(9):1339-1348. doi: 10.23736/S0022-4707.17.07409-6. Epub 2017 Jun 8. — View Citation

Zwolski C, Quatman-Yates C, Paterno MV. Resistance Training in Youth: Laying the Foundation for Injury Prevention and Physical Literacy. Sports Health. 2017 Sep/Oct;9(5):436-443. doi: 10.1177/1941738117704153. Epub 2017 Apr 27. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Fatigue The Fatigue Assessment Scale (FAS) is a unidimensional fatigue scale to rate how a person usually feels that is scored using a 5-point Likert scale from 1 (never) to 5 (always). It consists of 10 items, 9 of which were derived from four useful fatigue scales, namely the Checklist Individual Strength (CIS), the Emotional Exhaustion subscale from the Dutch version of the Maslach Burnout Inventory, the Energy and Fatigue subscale from the World Health Organization Quality of Life assessment instrument, and the Fatigue Scale. The satisfactory reliability and content validity of FAS were confirmed. Moreover, this scale is short and easy to use. 10-22 no fatigue, 22-34 mild fatigue, 35-50 severe 4 weeks
Primary Strength 1RM The one-repetition maximum (1RM) is the heaviest weight that can be lifted just once while using proper form. There are a number of benefits of the 1RM test over traditional laboratory testing. The 1 repetition maximum test more accurately reflects the dynamic muscle actions that are most typically utilized in resistance training and of natural movement in most activities of sport and daily life since eccentric actions are usually paired with concentric actions. Strength in compound movements can be evaluated with the 1RM test. The "gold standard" of dynamic strength tests, according to many studies. One study conducted in the year 2020 found that ICCs might be anywhere from 0.64 to 0.99 (median ICC = 0.97), with the vast majority (92%) having values below 0.90 and the vast majority (97%) having values below 0.80. CVs were observed between 5% and 12.1 % (median CV = 4.2 %) 4 weeks
Primary Gait parameters Cadence (no. of step/time)
Stride length (cm) distance of heel of right to heel of right
Step length (cm) initial contact of one foot to initial contact of opposite foot
Step width (cm) distance between two heels Speed (m/sec) distance/ time
4 weeks
See also
  Status Clinical Trial Phase
Terminated NCT03781817 - Intranasal Versus Intravenous Ketamine for Procedural Sedation in Children With Non-operative Fractures Phase 4
Recruiting NCT05424757 - Polyethylene Glycol Safety in Children
Recruiting NCT04602429 - Children's Acute Surgical Abdomen Programme
Completed NCT04933734 - Turkish Cultural Adaptation, Validity and Reliability of the "Physical Activity-Specific Rumination Scale for Children"
Completed NCT03457688 - Effect of Prebiotic Fructans to Reduce Number of Febrile Infections in Children N/A
Recruiting NCT05113420 - The Efficacy and Safety of Different Phlebotonic Drugs in Children With Venous Malformations
Completed NCT03241355 - Prebiotic Fructans on the Incidence of Acute Infectious Diseases in Children N/A
Not yet recruiting NCT05484102 - Preventive Effect of Cow's Milk Fermented With Lactobacillus Paracasei CBA L74 on Common Infectious Diseases in Children N/A
Recruiting NCT04460313 - Nasopharyngeal Carriage of S. Pneumoniae N/A
Not yet recruiting NCT05974917 - Serious gaMes as Emerging E-health Interventions for Young People With neurologicaL or rEspiratory disoRders
Completed NCT04057612 - Correlation Between Core Temperature and Skin Temperature in Pediatrics
Completed NCT04256590 - Tongue Depressor-related Tongue Swelling
Recruiting NCT03319927 - Reducing Pesticide Exposures in Child Care Centers N/A
Enrolling by invitation NCT05513235 - Feasibility Study of a Mobile Digital Personal Health Record for Family-Centered Care Coordination for Children and Youth With Special Healthcare Needs N/A
Completed NCT04615000 - SeroCovid<19: Covid-19 Seroconversion in Tertiary Pediatric Patients
Not yet recruiting NCT05568849 - Optical Coherence Tomography Angiography (OCTA) in Children's Cardiac Surgery N/A
Recruiting NCT06157346 - Characteristics of Intestinal Bacteria and Their Effects on Growth and Immune Function in Children at High Altitude
Recruiting NCT04206956 - Anxiety and Chronic Postsurgical Pain Following Ambulatory Surgery in Children
Completed NCT04315220 - Corestability Training in Overweight Children N/A
Recruiting NCT05043870 - Combined Immunosuppression for Pediatric Crohn's Disease Phase 4