- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00825903
The Effects of Exercise on Physiological and Psychological Parameters in an Asthmatic Population
Panoramica dello studio
Descrizione dettagliata
The study will run from August 2008 to May 2009. Recruitment and screening of participants will occur from August to December 2008 for inclusion into the clinical trial. Prior to the clinical trial participants will have a one hour informational session to clearly present the study, obtain signed informed consent and set up fitness/blood appointments for data collection. Data collection will begin the first week of school in January. The 12-week exercise protocol will start the second week of school and continue through the middle of April. Research participants will not have any exercise session during spring break (March 16-20). Final data collection will occur during the last two weeks of school. Pre-treatment and post-treatment data collection will include a fitness assessment and blood draw. Medication usage for asthma will be monitored on a weekly basis thoughout the clinical trial. Physical activity will also be monitored monthly.
The screening session is a 30-minute session where research participants complete health/behavior questionnaires and a physiological measure of lung function. Information to be collected in the health/behavior questionnaires includes: demographic and behavioral/lifestyle variables (sex, race, age, smoking status, and medical history).
The fitness assessment will be 60 minutes in length. At the beginning of the session participants will complete a survey to assess state anxiety (State-Trait Anxiety Inventory - Trait version Form X-1; Spielberger, Gorsuch, & Lushene, 1970). Heart rate variability will be measured through the ventral placement of 3 electrodes placed on the subject's torso. The areas will be prepped by swabbing with alcohol and lightly scrubbing to remove dead skin. The electrodes will be held in place with a sticky disc and a strip of athletic tape. Heart rate and resting blood pressure will also be taken. Body composition will be assessed using the BodPod system. Research participants will sit in an enclosed capsule (bod pod) for three tests lasting approximately 40 seconds each. Lung function will be assessed using a spirometer to measure the maximal volume of air exhaled over a period of time after a maximal inhalation. To assess cardiorespiratory fitness research participants will complete a VO2 Max test. Participants will ride a bicycle ergometer for approximately 15-20 minutes moving through stages (including a 3 minute warm-up) with progressively higher resistance levels until maximum tolerance. After termination there is a cool-down/recovery period of approximately 3-4 minutes.
The blood draw session will take approximately 30 minutes and participants will be asked to fast (no food or drink) for 12 hours prior to blood draw. Upon check-in participants will complete a series of questionnaires assessing psychological variables stress (Perceived Stress Scale-14 item version Form X-1; Cohen, Kamarck & Mermelstein, 1983), depression (Center for Epidemiological Studies - Depression Scale; Radloff, 1977), and quality of life (Asthma Impact Survey; QualityMetric Health Outcomes Solutions, Lincoln, RI). The quality and quantity of sleep will also be assessed using the Pittsburgh Sleep Quality Index (Buysse, Reynolds, Monk, Berman, & Kupfer, 1989). Once questionnnaires are completed, participants will have their blood drawn by a certified phlebotomist. Three days after the blood draw particpants will be contacted by phone and questioned about current health status.
After the first week of pretreatment data collection, before the training sessions begin, research participants will undergo an explanation and training session to learn how to evaluate their own rate of perceived exertion (RPE). The water-based exercise programs are 3 times a week for 12 weeks. The exercise sessions will begin with a 10-minute warm up and end with a 5-minute cool down period. The conditioning portion of the exercise program will be shorter in duration with lower intensities at the beginning of the 12 weeks. There will be a progression to higher intensities for longer periods of time throughout the 12 weeks using recommendations from the American College of Sports Medicine. Exercise sessions will not exceed 50 minutes.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
-
Washington
-
Pullman, Washington, Stati Uniti, 99164
- Washington State University
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Medically diagnosed and medication managed asthmatics between the ages of 18-40
Exclusion Criteria:
- outside the age range of 18-40 years old, fear of water, diseases or conditions listed during screening process, or current smoker.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: 1
Aquatic based exercise
|
Exercise 3 times each week for a total of 12 weeks.
Each session is 50 min.
in length.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Pulmonary Function
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Storia medica
Lasso di tempo: linea di base
|
linea di base
|
|
Demographic information
Lasso di tempo: baseline
|
baseline
|
|
Smoking practices
Lasso di tempo: baseline
|
baseline
|
|
Exercise practices
Lasso di tempo: baseline and monthly
|
baseline and monthly
|
|
State Anxiety
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Perceived Stress
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Depression
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Sleep - duration and quality
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Quality of Life as related to asthma
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Body composition
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Cardiovascular fitness level- VO2 max
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Resting Heart Rate
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Heart Rate Variability and ECG
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Serum cholesterol levels
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Fasting blood glucose
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Cortisol
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Insulin
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
CRP
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Homocysteine
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Lipoprotein-Associated Phospholipase A2 (PLAC)
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
|
Medication usage
Lasso di tempo: prior and throughout study
|
prior and throughout study
|
|
Exercise Adherence
Lasso di tempo: throughout study
|
throughout study
|
|
Resting blood pressure
Lasso di tempo: baseline and 12 weeks post
|
baseline and 12 weeks post
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Kasee J Hildenbrand, PhD, Washington State University
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 10460
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