Informazioni generali
  • Categoria della malattia Lesione / ferita (BASEC)
  • Fase dello studio N/A (ICTRP)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Winterthur
    (BASEC)
  • Responsabile dello studio Michelle C. Haas michelle.haas2@zhaw.ch (BASEC)
  • Fonte dati BASEC: Importato da 07.03.2025 ICTRP: Importato da 20.03.2025
  • Ultimo aggiornamento 20.03.2025 02:00
HumRes66324 | SNCTP000006266 | BASEC2024-01173 | NCT06845150

Combined mental and physical training in an immersive environment compared to sequential mental and physical training in individuals with reconstructed anterior cruciate ligament

  • Categoria della malattia Lesione / ferita (BASEC)
  • Fase dello studio N/A (ICTRP)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Winterthur
    (BASEC)
  • Responsabile dello studio Michelle C. Haas michelle.haas2@zhaw.ch (BASEC)
  • Fonte dati BASEC: Importato da 07.03.2025 ICTRP: Importato da 20.03.2025
  • Ultimo aggiornamento 20.03.2025 02:00

Descrizione riassuntiva dello studio

Anterior cruciate ligament tears commonly occur in sports and lead to a rehabilitation time of up to one year. Individuals after an ACL tear show a persistently altered movement pattern and deficits in mental functions such as reaction inhibition. However, when individuals are in an immersive environment after an ACL tear, their movement pattern resembles that of healthy individuals. Dual-task training, a combined mental and physical training, improves mental functions in female team sport athletes. Therefore, dual-task training in an immersive environment, for example through exergaming, offers great potential to improve these factors. Thus, we investigate in this study what changes occur in mental and physical functions, as well as in motivation, when training with or without dual-task for 10 weeks. We also examine how dual-task training in an immersive environment affects biomechanical movement patterns. The aim of this study is to investigate how physical and mental functions change when training with or without dual-task for 10 weeks, how intrinsic motivation changes over 10 weeks, and how dual-task training in an immersive environment affects biomechanical movement patterns. Individuals aged between 18 and 40 years who have had an ACL tear at least six months ago and have received clearance for single-leg jumps will be recruited for the study. In a first appointment, physical and mental tests will be conducted. In a second appointment, biomechanics will be measured during immersive dual-task training. Participants will then be randomly divided into two groups. For 10 weeks, participants will either complete an individually guided training or a dual-task training twice a week. In a final appointment, the tests will be repeated to observe differences compared to the first.

(BASEC)

Intervento studiato

dual-task training

(BASEC)

Malattie studiate

Return to competition after cruciate ligament rupture

(BASEC)

Criteri di partecipazione
- 18-40 years old - at least 6 months since an anterior cruciate ligament tear - written consent of the treating surgeon to undertake the training (BASEC)

Criteri di esclusione
- Surgery on the non-injured leg in the last 12 months - Concussion in the last 6 months - Inflammatory pain or severe swelling during exercise (BASEC)

Luogo dello studio

Winterthur

(BASEC)

Switzerland (ICTRP)

Sponsor

non disponibile

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Michelle C. Haas

+41589347557

michelle.haas2@zhaw.ch

(BASEC)

Informazioni generali

+41 58 934 75 57

michelle.haas2@zhaw.ch

(ICTRP)

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione etica Zurigo

(BASEC)

Data di approvazione del comitato etico

04.02.2025

(BASEC)


ID di studio ICTRP
NCT06845150 (ICTRP)

Titolo ufficiale (approvato dal comitato etico)
non disponibile

Titolo accademico
Dual-Task Training in an Immersive Environment Compared to Single Task Training in Anterior Cruciate Ligament Reconstructed Individuals (ICTRP)

Titolo pubblico
Combined Compared to Sequential Cognitive and Physical Training in Anterior Cruciate Ligament Reconstructed Individuals (ICTRP)

Malattie studiate
Anterior Cruciate Ligament Reconstruction Rehabilitation (ICTRP)

Intervento studiato
Other: Dual-task trainingOther: Single task training (ICTRP)

Tipo di studio
Interventional (ICTRP)

Disegno dello studio
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: None (Open Label). (ICTRP)

Criteri di inclusione/esclusione
Inclusion Criteria:

- 18-40 years old

- At least 6 months after ACL injury

- Surgically reconstructed ACL

- At least 2 hours of sports participation before the injury

- Written consent of the attending surgeon to perform intensified training methods
including one-legged jumps at 6 months after surgery after the first visit

- Ability to give informed consent as documented by signature

- Ability to understand instructions in German or English

- BMI < 28 kg/m^2

- Availability to take part in at least 70% of all training sessions

Exclusion Criteria:

- Surgery on the contralateral leg during the last 12 months

- Acute or chronic musculoskeletal, neurological, or cardiopulmonary disorders

- Unadjusted vision problems

- Concussion during the last 6 months

- Pregnancy

- Breastfeeding

- Amputation

- Inflammatory pain or swelling during exercising (ICTRP)

non disponibile

Endpoint primari e secondari
Interference;Response inhibition (ICTRP)

Jumping performance - contact time;Jumping performance - peak force;Strength;Intrinsic motivation;Kinematics of the lower extremities (ICTRP)

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
Kantonsspital Winterthur KSW;ZHAW DIZH Fellowship Program (ICTRP)

Contatti aggiuntivi
Michelle C. Haas, michelle.haas2@zhaw.ch, +41 58 934 75 57 (ICTRP)

ID secondari
DUACL (ICTRP)

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
https://clinicaltrials.gov/ct2/show/NCT06845150 (ICTRP)


Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile