- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07845968
Comparative Effects of Advanced Neuromuscular and Dynamic Balance Training Among Hockey Players
Comparative Effects of Advanced Neuromuscular and Dynamic Balance Training on Strength , Balance and Functional Performance Among Hockey Players
This randomized clinical trial aims to compare the effects of advanced neuromuscular training and dynamic balance training on strength, balance, and functional performance among male hockey players. A total of 34 participants will be randomly allocated into two intervention groups. Both groups will receive supervised training sessions three times per week for six weeks. Outcomes including lower limb strength, dynamic balance and agility will be assessed before and after the intervention using validated assessment tools. The findings of this study will help determine which training approach is more effective for improving athletic performance and reducing the risk of injury in hockey players.
Studienübersicht
Status
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Punjab Province
-
Gojra, Punjab Province, Pakistan, 36120
- Gojra Hockey Stadium
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
-
• Male participants aged 18 to 25 years. (34)
- Participants must be licensed, competitive hockey players (field or ice hockey) actively engaged in league play or elite training. (29)
- Participants should have a minimum of one year of competitive hockey experience. (35)
- Free from lower limb injuries for a minimum of six months before assessment. (6)
- No prior functional/neuromuscular training experience. (36)
- Participants should be actively participating in physical activity for at least 30 minutes per day, three days per week. (37)
Exclusion Criteria:
-
• History of musculoskeletal injuries within the past 12 months.
- Medical conditions that could limit involvement in training or influence assessment results. (29)
- Recent involvement in other balance or neuromuscular training programs. (17)
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: ADVANCED NEUROMUSCULAR TRAINING
Participants in this group receive an advanced neuromuscular training program focusing on strength, proprioception, agility, and coordination exercises. The training includes progressive drills designed to improve neuromuscular control, dynamic stability, and functional performance. Sessions are conducted under supervision over the study duration as per protocol. |
A structured advanced neuromuscular training program including strength, proprioception, agility, and coordination exercises aimed at improving neuromuscular control and dynamic stability. The program is conducted under supervision according to the study protocol. |
|
Aktiver Komparator: DYNAMIC BALANCE TRAINING
Participants in this group receive a dynamic balance training program consisting of exercises aimed at improving postural control, balance, and stability during movement. The program includes dynamic tasks such as balance board activities and controlled movement exercises performed under supervision throughout the study period. |
A dynamic balance training program consisting of exercises designed to improve postural control, balance, and movement stability. The training includes dynamic tasks performed under supervision throughout the study period. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Star Excursion Balance Test
Zeitfenster: [Time Frame: 6 weeks]
|
It is a dynamic balance test that assesses neuromuscular control and postural stability during multi-directional reaching tasks while standing on one leg. It demonstrates high reliability (ICC = 0.85-0.96) and good validity in identifying lower limb deficits, especially following ankle sprains and in athletic populations. Pre and post assessment will be done. |
[Time Frame: 6 weeks]
|
|
Single-Leg Hop Distance
Zeitfenster: [Time Frame: 6 weeks]
|
It evaluates single-leg functional performance by measuring the maximum horizontal distance achieved during a single forward hop on one leg. The Single-Leg Hop Test will be used to assess lower limb functional performance and dynamic control. The hopping distance will be measured in centimeters (cm). Pre and post assessment will be done. |
[Time Frame: 6 weeks]
|
|
Triple Hop Distance
Zeitfenster: [Time Frame: 6 weeks]
|
It evaluates single-leg functional performance by measuring the maximum horizontal distance achieved during three consecutive forward hops on the same leg. The Triple Hop Test will be used to assess lower limb functional performance, power, and dynamic stability. The total hopping distance will be measured in centimeters (cm). Pre and post assessment will be done. |
[Time Frame: 6 weeks]
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Sidra Shafique, MS, Riphah International University
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- REC/RCR & AHS/25/0440
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .