Jumping Exercises Approach in Individuals With Chronic Ankle Instability
The Effect of a 12-week Training Jumping Exercises Program in Individuals With Chronic Ankle Instability: Randomized Controlled Trial Pilot Study
Przegląd badań
Status
Interwencja / Leczenie
Szczegółowy opis
There is a need for;
- more homogeneous sub- groups with chronic functional instability of the ankle.
- Studies are needed that older patients (up to 50 years) and also take into account women.
- In addition, studies should be performed in a clinical environment and also at the same time clinically adapted test can be used as a form measurement.
( Hiller et al. , 2011).
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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ZH
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Zurich, ZH, Szwajcaria, 8008
- Balgrist Univeresty Hospital
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Ankle injury more than 6 months ago
- Chronic instability
- Functional instability of the ankle
- Experience with proprioceptive exercises
Exclusion Criteria:
- Foot surgery
- Fresh ankle injury
- Acute foot pain with signs of inflammation
- Mechanical / anatomical ankle instability
- Athletes with regularly jumping exercise (eg volleyball, basketball)
- Taking medications which affect balance and coordination
- Diseases that affect the balance
- Serious diseases such as tumors, infections, neuropathies, severe articular degeneration
- Non-German-speaking patients
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Jumping exercise
Physical therapy with a focus on specific jumping exercise. The jumping exercise will be performed for 12 weeks (3x/week), with a break of day between workouts. The 40-minute workout is completed 2 times under supervision in the clinic's internal training group for outpatients. 1 time they train on their own at home, based on a defined training program. The training process is documented by the training protocol. The incipient exercise intensity is taking personal performance into account. The exercise intensity is increased by a progressive scheme. |
Total 120min exercise
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Aktywny komparator: Strength exercise
Physical Therapy with a focus on stability and strength exercise. Strength exercise arm has also same duration of 12 weeks with comparable intensity. The program is according to a predetermined program. The 60-minute training is completed twice under supervision in the clinic's internal training group for outpatients.There is no contact with participants of other group. Between the two exercise sessions there is a training free day. The training process is documented by the training protocol. The incipient exercise intensity is considering personal performance. The intensity is increased after workout usual principles. The exercises are described with clear image and load parameters. The training exercises are regularly monitored. |
Total 120 min exercise
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change from Baseline in Gait variables
Ramy czasowe: Change from Baseline in Gait variables at week 3, week 7, and at the end of therapy (week 12)
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Gait variables will be assessed with the OptoGait system OptoGait system is a floor-based photocell system for measuring spatiotemporal gait parameters. All measurements will be executed within 1hour |
Change from Baseline in Gait variables at week 3, week 7, and at the end of therapy (week 12)
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Balance
Ramy czasowe: Baseline, week 3, week 7, and at the end of therapy (week 12)
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Time to Stability (Forceplate Accusway AMTI)
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Baseline, week 3, week 7, and at the end of therapy (week 12)
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Health questionnaire
Ramy czasowe: Baseline, week 3, week 7, and at the end of therapy (week 12), followup 12 months
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EQ-5D is a standardised instrument for use as a measure of health outcome.
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Baseline, week 3, week 7, and at the end of therapy (week 12), followup 12 months
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Foot function questionnaire
Ramy czasowe: Baseline, week 3, week 7, and at the end of therapy (week 12)
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The Foot and Ankle Ability Measure (FAAM) is a self-report outcome instrument developed to assess physical function for individuals with foot and ankle related impairments.
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Baseline, week 3, week 7, and at the end of therapy (week 12)
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Personal calendar
Ramy czasowe: 12 months
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Participant could enter any new ankle sprain into this calendar.
As soon as possible after new ankle sprain the participant had to fill in the date, its cause, and sprain-related injuries.
The calendar pages contained questions about the circumstances surrounding the new ankle sprain, including how and where it happened, activity performed, possible injury symptoms, time to recover and whether medical assistance or physical therapy was needed.
Participants are also requested to record direct medical costs (e.g.
physiotherapy, visits to general practitioners and medical specialists, nursing care, and medication) and indirect cost (e.g.
disability related loss) using the "personal calendar".
At the end of 2 month, a calendar page was sent by each patient to the investigators
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12 months
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Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Jaap Swanneburg, PhD, Balgrist Univeresty Hospital
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- Balgrist 2009-124
- KEK-ZH-Nr. 2009-124 (Inny identyfikator: Ethics commission of the Canton Zurich, Switzerland)
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
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