High-intensity Training for Improving Physical Performance of Aged Women (AHIITATE)
4. März 2019 aktualisiert von: María Carrasco Poyatos, Universidad de Almeria
Effects of High-intensity Interval Circuit Training (HIICT) on the Cardiovascular and Functional Parameters of Aged Women
This study evaluates the adaptations on the functional capacity and cardiovascular in elderly after a physical activity program circuit training.
The participants were divided into three groups: Circuit training based on high-intensity interval training group (HIICT), Circuit training at moderate intensity group (MICT) and Control group (CG).
Studienübersicht
Status
Abgeschlossen
Bedingungen
Detaillierte Beschreibung
Three groups of participants (circuit training based on high-intensity interval training, circuit training at moderate intensity and not training group) will enter the study. The intervention will consist of a physical exercise program in day centers.
Intensity progression will be encouraged according to the rate of perceived exertion. Progression of exertion will be "very hard", "extremely hard" and "maximal exertion" for HIT group, and "light", "somewhat hard" and "hard" for group. Assessment will be undertaken at two-time points: baseline and after 16 weeks of exercise training.
Assessment will include VO2 peak, functional capacity, health-related quality of life, cognitive state and daily physical activity.
Studientyp
Interventionell
Einschreibung (Tatsächlich)
54
Phase
- Unzutreffend
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
50 Jahre bis 90 Jahre (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Ja
Studienberechtigte Geschlechter
Weiblich
Beschreibung
Inclusion Criteria:
- Having 50 - 90 years old.
- Not suffering chronic heart, respiratory or joint disease, taking medication or having a deteriorated level of mental health that could interfere in carrying out exercise programs.
- Having 0 or 1 responses positive in the Physical Activity Readiness Questionnaire (ParQ). Only item 6, related to mild vascular diseases.
- Being physically independent according to the scales Lawton and Brody, and Katz.
Exclusion Criteria:
- Having uncontrolled arterial hypertension.
- Having practiced during the previous 3 months or practicing at present a similar exercise to the one proposed in the study.
- Attending sessions less than 80%.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Grundlegende Wissenschaft
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: High-intensity interval training group
Frequency: 2 days/weeks; Intensity: 16-18 Börg/85-100%VO2max; Recovery: Active; Duration: 1 hour.
|
16 weeks of High-intensity interval training
|
|
Experimental: Moderate-intensity interval training group
Frequency: 2 days/weeks; Intensity: 12-14 Börg/60-70% VO2max; Recovery: Active; Duration: 1 hour.
|
16 weeks of Moderate-intensity interval training
|
|
Kein Eingriff: Control group
Maintain their normal daily activities throughout the sixteen-week experimental period.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Analyses changes in maximum oxygen consumption (VO2max).
Zeitfenster: Pre and post after sixteen weeks of intervention
|
A modified Balke treadmill protocol will be used to estimate aerobic capacity (VO2max).
|
Pre and post after sixteen weeks of intervention
|
|
Analyses changes in maximum oxygen consumption (VO2max).
Zeitfenster: Pre and post after sixteen weeks of intervention
|
VO2max was assessed using the 6-Minute Walk Test.
The participant should walk the longest distance possible in 6 minutes by walking continuously the 42 metres indicated on the floor.
It measures the distance in meters
|
Pre and post after sixteen weeks of intervention
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Analyses changes in heart rate reached in ergometry.
Zeitfenster: Pre and post after sixteen weeks of intervention
|
Analyses during modified Balke treadmill protocol
|
Pre and post after sixteen weeks of intervention
|
|
Analyses changes in blood pressure reached in ergometry.
Zeitfenster: Pre and post after sixteen weeks of intervention
|
Analyses during modified Balke treadmill protocol
|
Pre and post after sixteen weeks of intervention
|
|
Analyses changes in maximum speed reached in ergometry.
Zeitfenster: Pre and post after sixteen weeks of intervention
|
Analyses during modified Balke treadmill protocol
|
Pre and post after sixteen weeks of intervention
|
|
Analyses changes in duration test reached in ergometry.
Zeitfenster: Pre and post after sixteen weeks of intervention
|
Analyses during modified Balke treadmill protocol
|
Pre and post after sixteen weeks of intervention
|
|
Analyses changes in fat percentage.
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
Fat percentage (%) was assessed using bioimpedance analysis (OMROM BF-306).
|
Pre and post after sixteen weeks of intervention.
|
|
Analyses changes in body mass index (BMI).
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
BMI was assessed using bioimpedance analysis (OMROM BF-306).
|
Pre and post after sixteen weeks of intervention.
|
|
Analyses changes in gait.
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
Gait was assessed using the Timed Up and Go Test.
To stand up from a standard arms chair, walk 3 meters, turn back the cone walk back and sit down to the chair.
The time in seconds is record.
|
Pre and post after sixteen weeks of intervention.
|
|
Analyses changes in balance.
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
Balance was assessed using the One Leg Standing Test.
This test consist in maintain one leg stance for as long as possible.
The test was considered normal if the one leg standing time reached 30 seconds.
|
Pre and post after sixteen weeks of intervention.
|
|
Analyses changes in lower body strength.
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
Lower body strength was assessed using the Sit To Stand 30.
For the Sit To Stand 30, the participant consist in measures how many repetition the participant can to stand up and sit down during 30 seconds.
|
Pre and post after sixteen weeks of intervention.
|
|
Analyses changes in upper body strength.
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
Upper body strength was assessed using the Arm Curl Test (30).
For this test, the participant consist in measures how many repetition the participant can to curl up and curl down during 30 seconds.
|
Pre and post after sixteen weeks of intervention.
|
|
Analyses changes in maximal handgrip strength.
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
To measure the amount of strength developed by each hand in kg.
|
Pre and post after sixteen weeks of intervention.
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Analyses change in Self Assessed Physical Activity.
Zeitfenster: Pre and post after sixteen weeks of intervention.
|
Physical activity was assessed using the Physical Activity Scale of the Elderly (PASE) questionnaire.
The PASE is designed to assess physical activity in older persons.
The total PASE score was computed by multiplying the amount of time spent in each activity (hours/week) or participation (yes/no) in an activity by empirically derived item weights and summing over all activities.
PASE scores for this study ranged from 0 to 756 with higher scores indicating more physical activity.
|
Pre and post after sixteen weeks of intervention.
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Ermittler
- Hauptermittler: Ismael Ballesta García, PhD. Student, Universidad de Almeria
- Hauptermittler: María Carrasco Poyatos, PhD., Universidad de Almeria
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Allgemeine Veröffentlichungen
- Wisloff U, Stoylen A, Loennechen JP, Bruvold M, Rognmo O, Haram PM, Tjonna AE, Helgerud J, Slordahl SA, Lee SJ, Videm V, Bye A, Smith GL, Najjar SM, Ellingsen O, Skjaerpe T. Superior cardiovascular effect of aerobic interval training versus moderate continuous training in heart failure patients: a randomized study. Circulation. 2007 Jun 19;115(24):3086-94. doi: 10.1161/CIRCULATIONAHA.106.675041. Epub 2007 Jun 4.
- Guiraud T, Juneau M, Nigam A, Gayda M, Meyer P, Mekary S, Paillard F, Bosquet L. Optimization of high intensity interval exercise in coronary heart disease. Eur J Appl Physiol. 2010 Mar;108(4):733-40. doi: 10.1007/s00421-009-1287-z.
- Huang SC, Wong MK, Lin PJ, Tsai FC, Fu TC, Wen MS, Kuo CT, Wang JS. Modified high-intensity interval training increases peak cardiac power output in patients with heart failure. Eur J Appl Physiol. 2014 Sep;114(9):1853-62. doi: 10.1007/s00421-014-2913-y. Epub 2014 Jun 1.
- Ballesta Garcia I, Rubio Arias JA, Ramos Campo DJ, Martinez Gonzalez-Moro I, Carrasco Poyatos M. High-intensity Interval Training Dosage for Heart Failure and Coronary Artery Disease Cardiac Rehabilitation. A Systematic Review and Meta-analysis. Rev Esp Cardiol (Engl Ed). 2019 Mar;72(3):233-243. doi: 10.1016/j.rec.2018.02.015. Epub 2018 Apr 9. English, Spanish.
Nützliche Links
- Carrasco, M., Navarro, M.D., Martínez, I., Reche-Orenes, D. (2016). Daily physical activity impact in old women bone density and grip strength. Nutrición Hospitalaria, 33(6), 1305-1311.
- Carrasco, M., Martínez, I., Navarro, M.D. (2015). Daily physical activity and bone mineral density in older women. Revista Brasileira de Medicina do Esporte, 21(1), 22-26.
- Carrasco, M., Vaquero, M. (2012). Water training in postmenopausal women: effect on muscular strength. European Journal of Sport Science, 12(2), 193-200.
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
20. Dezember 2015
Primärer Abschluss (Tatsächlich)
1. Februar 2016
Studienabschluss (Tatsächlich)
20. Juni 2016
Studienanmeldedaten
Zuerst eingereicht
5. September 2018
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
11. Februar 2019
Zuerst gepostet (Tatsächlich)
15. Februar 2019
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
6. März 2019
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
4. März 2019
Zuletzt verifiziert
1. März 2019
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- HIICT-OW/16
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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