The effect of low volume Nordic hamstring exercise on physical performance in amateur youth football players

ISRCTN ISRCTN34441474
DOI https://doi.org/10.1186/ISRCTN34441474
Secondary identifying numbers 00052134042112620220813090
Submission date
19/09/2022
Registration date
23/09/2022
Last edited
12/08/2024
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Background and study aims
Nordic Hamstring Exercise (NHE) is an effective hamstring injury prevention program but has low compliance issues among amateur and elite football players. Studies showed that Low volume NHE results in similar structural changes in muscle and is suggested as an alternative program with less side effects of Delayed Onset Muscle Soreness (DOMS), a factor that influences compliance. Another approach to convince the coaches and players of the program is to provide evidence of the program's effect on physical performance. Promoting the performance-enhancing effects may motivate them to implement the program consistently. The primary aim of this study is to determine the effects of the 8-week low volume of the NHE program on physical performance, which includes eccentric hamstring strength, sprint, vertical jump, and Change of Direction (CoD) performance in amateur male academy football players. In addition, we aim to investigate muscle soreness as a potential side effect of intervention experienced by subjects using the Numerical Rating Scale (NRS) for hamstring pain.

Who can participate?
This study requires 40 healthy male amateur youth football players aged 14-17 years old.

What does the study involve?
This is a randomized controlled trial (RCT) with 2-group parallel design. The intervention is a supervised 8-week low-volume Nordic Hamstring Exercise/NHE protocol (NHE group), and the control will perform the regular football training (CON group). The primary endpoints are change of eccentric hamstring strength, 30-m sprint, vertical jump, and CoD performance from baseline that will be recorded at an 8-week follow-up.

What are the possible benefits and risks of participating?
Benefit: The Low Volume Nordic Hamstring Exercise Program has a potential effect on improving football performance, but that is not certain. By participating, subjects contribute to knowledge with which we can better football performance in the future.
Risk: The program is not considered risky because they are existing exercises that are already used in daily practice. Especially at the beginning of the program, some muscle pain/soreness is often reported.

Where is the study run from?
Faculty of Sports Science, Universitas Negeri Yogyakarta, Indonesia
Faculty of Sports Science, Universitas Negeri Surabaya, Indonesia
Department of Orthopedic Surgery and Sports Medicine, Amsterdam UMC, The Netherlands

When is the study starting and how long is it expected to run for?
June 2022 to June 2023

Who is funding the study?
Investigator initiated and funded
This trial is supported by the Indonesia Endowment Fund for Education, Ministry of Finance, Republic of Indonesia, for Ph.D. program scholarship.

Who is the main contact?
Muhammad Ikhwan Zein, m.i.zein@amsterdamumc.nl

Contact information

Mr Muhammad Ikhwan Zein
Scientific

Jacques Veltmanstraat 793
Amsterdam
1065 DZ
Netherlands

ORCiD logoORCID ID 0000-0003-3728-5065
Phone +31 648419199
Email m.i.zein@amsterdamumc.nl

Study information

Study designRandomized superiority controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Other
Study typeOther, Efficacy
Participant information sheet Not available in web format, please use the contact details to request a patient information sheet.
Scientific titleLow Volume Nordic Hamstring Exercise Research
Study acronymLOVENDER
Study objectivesWe hypothesize that eight weeks of the low volume Nordic Hamstring Exercise (NHE) provide sufficient time to allow the physiological adaptation and contribute positive effect on eccentric hamstring strength, sprint, vertical jump and Change of Direction (COD)

Our secondary hypothesis is subjects in the intervention group will experience a very low level of hamstring pain as a side effect of the program
Ethics approval(s)Approved 22/08/2022, Ethics Commission Universitas Negeri Yogyakarta (Jl. Colombo No. 1. Caturtunggal, Kec. Depok, Kabupaten Sleman, Daerah Istimewa Yogyakarta, Indonesia; +62 274 586168; lppm@uny.ac.id), ref: No.B/46/UN.34.21/TU/2022
Health condition(s) or problem(s) studiedHealthy male amateur youth football players
InterventionRandomization
Subjects are stratified by the football team and individually randomized to the Intervention (NHE)- or control group with the 1:1 allocation ratio using an online software application (sealed envelope™).

Intervention
Subjects in the NHE group will perform low volume NHE program in addition to their regular football training, while the CON group will only perform their regular football training. It consists of 10 sessions in 8 weeks of follow-up (144 reps of total volume and 21 reps of average weekly volume).

Study Setting
The intervention will be conducted during the regular football training schedule. The data collection procedures will be performed in a similar condition on the same football field with the same trained staff/tester.

Data Collection
Subject characteristics, including age (year), height (m), weight (kg), and BMI (kg/m2), will be collected in both groups. The physical performance tests as the primary outcome will be conducted twice, before and after the eight weeks of intervention.
Intervention typeBehavioural
Primary outcome measure1. Eccentric hamstring strength is measured using Hamstring Testing System (Nordboard) at baseline and week 9
2. 30 meter sprint is measured using speed recording system based on the light sensors (fitlight) at baseline and week 9
3. Vertical jump is measured using dual forceplate system (Vald Forcedecks) at baseline and week 9
4. Change of Direction (CoD) is measured using speed recording system based on the light sensors (fitlight) at baseline and week 9
Secondary outcome measuresPain is measured using a Numerical Rating Scale after the intervention has performed (twice a week for 2 weeks then continue once a week for 6 weeks)
Overall study start date01/06/2022
Completion date30/06/2023

Eligibility

Participant type(s)Healthy volunteer
Age groupOther
Lower age limit14 Years
Upper age limit17 Years
SexMale
Target number of participants40
Total final enrolment72
Key inclusion criteria1. Male football players
2. Aged 14-17 years
3. Active participation in the football academy
Key exclusion criteria1. History of back and lower extremity injury (including hamstring) in the previous six months prior to the study
2. Specific eccentric strength training and specific sprint training more than one session per week in the previous six weeks prior to the study
3. Sustain injury during intervention period
4. Compliance < 75% of the total program
5. Absence in the pre- and/or-post test
Date of first enrolment27/09/2022
Date of final enrolment30/06/2023

Locations

Countries of recruitment

  • Indonesia

Study participating centres

Faculty of Sports Science, Universitas Negeri Yogyakarta
Jalan Colombo No.1 Karangmalang Yogyakarta
Yogyakarta
55281
Indonesia
Faculty of Sports Science, Universitas Negeri Surabaya
Lidah Wetan
Kec. Lakarsantri
Kota Surabaya
Jawa Timur
Surabaya
60213
Indonesia
Department of Orthopedic Surgery and Sports Medicine
Location AMC K1-208. Meibergdreef 9
Amsterdam
1105 AZ
Netherlands

Sponsor information

Ministry of Finance Republic of Indonesia
Government

Indonesia Endowment Fund for Education (Lembaga Pengelola Dana Pendidikan / LPDP)
Gedung Danadyaksa Cikini
Jl. Cikini Raya No.91A-D
Menteng
Jakarta
10330
Indonesia

Phone +62 2123951607
Email cso.lpdp@kemenkeu.go.id
Website https://lpdp.kemenkeu.go.id/en/

Funders

Funder type

Other

Investigator initiated and funded

No information available

Results and Publications

Intention to publish date01/12/2024
Individual participant data (IPD) Intention to shareYes
IPD sharing plan summaryAvailable on request
Publication and dissemination planThe results will be submitted for publication to an international, peer-reviewed journal, regardless of whether they will be positive, negative, or inconclusive in relation to the study hypothesis. The new knowledge will also be disseminated through websites, presentations, social media, and professional organizations (orthopedics and sports medicine, sports physiotherapists, athletic trainers, and public health).
IPD sharing planData are available upon reasonable request.
Data are deidentified participant data and it will be made available as soon as possible with publication. How to access data: m.i.zein@amsterdamumc.nl. Data will be shared, wherever legally and ethically possible an in line with ICMJE guidelines, with researchers who provide a methodologically sound proposal.

Editorial Notes

12/08/2024: The following changes were made to the trial record:
1. The overall end date was changed from 31/01/2023 to 30/06/2023.
2. The total final enrolment was added.
3. The recruitment end date was changed from 01/12/2022 to 30/06/2023.
4. The participant level data sharing statement was added.
5. The intention to publish date was changed from 01/11/2023 to 01/12/2024.
22/09/2022: Trial's existence confirmed by Ethics Commission Universitas Negeri Yogyakarta