- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01172327
Self-Directed Exercise Program for Adults With Arthritis
26 aprile 2021 aggiornato da: Sara Wilcox, University of South Carolina
Evaluation of a Self-directed, Packaged Physical Activity Program for Adults With Arthritis
The purpose of this study is to examine the effectiveness and safety of a self-directed physical activity program relative to a self-directed dietary program in adults with arthritis.
A process evaluation will also be conducted to examine program reach, participation/dose, fidelity, and participant compatibility/satisfaction.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Physical activity is a critical component of arthritis disease management.
It also reduces the risk for other chronic comorbid conditions in people with arthritis.
Yet, most adults with arthritis are not sufficiently active at the level needed to achieve benefits.
Existing group-based arthritis exercise programs reach only a very small percentage of the population.
The overall purpose of this study is to test a self-directed and low-cost multicomponent physical activity program for people with arthritis on outcomes including symptoms of arthritis, lower body strength, functional aerobic capacity, flexibility, physical activity, arthritis self-efficacy and disability, upper body strength, balance, gait, and depressive symptoms.
The second primary aim is to evaluate the safety of the physical activity program.
The third primary aim is to conduct a process evaluation to examine program reach, participation/dose, fidelity, and participant compatibility/satisfaction.
Adults aged 18 years and older with arthritis will be recruited from the midlands area of South Carolina.
After completion of a baseline visit, participants will be randomized in equal numbers to the 12-week physical activity program (First Step to Active Health®) or the 12-week attention-control group (Steps to Healthy Eating).
The attention control intervention will have the same "look and feel" as the physical activity intervention and will require similar activities such as self-monitoring of behavior.
Follow-up measurements will take place post-program (12-weeks) and 6 months post-program (i.e., 9 months post-randomization).
If First Step to Active Health® is shown to be effective, it could be widely disseminated for a very low cost, thus having the potential to make a tremendous public health impact on the burden of arthritis.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
401
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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South Carolina
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Columbia, South Carolina, Stati Uniti, 29208
- University of South Carolina Prevention Research Center
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
18 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion Criteria:
- Self-reported, health care provider-diagnosed arthritis (CDC definition)
- 18+ years of age
- Self-reported symptoms of joint pain, stiffness, tenderness, decreased range of motion, redness and warmth, deformity, crackling or grating, or fatigue
- Able to read and write in English
Exclusion Criteria:
- Another member of household is participating in study
- Plans to move from the Columbia, SC area in the next 9 months
- Unable to walk longer than 3 minutes without taking a rest
- Unable to stand without assistance for more than 2 minutes
- Cannot sit in a chair without arms for more than 5 minutes
- Measured resting blood pressure >160/100
- Positive response to PAR-Q question(s)
- Had a fall in the past year that required medical assistance
- Pregnant or breastfeeding
- Uses insulin to manage diabetes
- Participating in another research study that includes an intervention or drug
- Participates in 3+ days of structured moderate-intensity exercise for 30+ minutes per day
- Participates in 2+ days of strength building exercises for 20+ minutes per day
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Multicomponent exercise
This arm is a self-directed, multicomponent, exercise intervention.
Participants exercise on their own and follow a progressive stepped program that occurs in the following order: cardiorespiratory exercises, flexibility exercises, strength (upper and lower body) exercises, and balance exercises.
Participants also complete a daily log of their exercises and return the logs every week for 12 weeks.
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This intervention is a self-directed, multicomponent, exercise intervention.
Participants exercise on their own and follow a progressive stepped program that occurs in the following order: cardiorespiratory exercises, flexibility exercises, strength (upper and lower body) exercises, and balance exercises.
Participants also complete a daily log of their exercises and return the logs every week for 12 weeks.
The active intervention phase is 12 weeks.
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Comparatore attivo: Nutrition
This arm is a self-directed nutrition intervention.
Participants follow a progressive stepped program that occurs in the following order: fruits, vegetables, grains, meat and beans.
Participants also complete a daily log of their dietary intake and return the logs every week for 12 weeks.
|
This arm is a self-directed nutrition intervention.
Participants follow a progressive stepped program that occurs in the following order: fruits, vegetables, grains, meat and beans.
Participants also complete a daily log of their dietary intake and return the logs every week for 12 weeks.
The active intervention lasts for 12 weeks.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Symptoms of arthritis
Lasso di tempo: 12 weeks
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Visual numeric scales to assess pain, fatigue, and stiffness
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12 weeks
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Lower body strength
Lasso di tempo: 12 weeks
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The 30-second chair stand will assess lower body strength.
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12 weeks
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Functional exercise capacity
Lasso di tempo: 12 weeks
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The six-minute walk will assess functional exercise capacity
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12 weeks
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Flexibility
Lasso di tempo: 12 weeks
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The sit-and-reach test will assess flexibility
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12 weeks
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Physical activity
Lasso di tempo: 12 weeks
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The Community Health Activities Model Program for Seniors Physical Activity (CHAMPS) Questionnaire will assess physical activity participation
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12 weeks
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Arthritis management self-efficacy
Lasso di tempo: 12 weeks
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The Arthritis Self-Efficacy Scale will assess confidence in managing arthritis symptoms
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12 weeks
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Disability
Lasso di tempo: 12 weeks
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The Health Assessment Questionnaire (HAQ) will assess disability
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12 weeks
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Upper body strength
Lasso di tempo: 12 weeks
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The grip strength test (kg/lbs of force) will assess upper body strength
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12 weeks
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Balance
Lasso di tempo: 12 weeks
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Postural sway will be measured with the AMTI force platform to determine COP displacement, COP velocity, and 95th eclipse
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12 weeks
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Gait
Lasso di tempo: 12 weeks
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GAITRite will assess components of gait including cadence, step time, cycle time, step length, stride length, and velocity
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12 weeks
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Depressive symptoms
Lasso di tempo: 12 weeks
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The short form of the Center for Epidemiological Studies Depression scale (CES-D) will assess depressive symptoms
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12 weeks
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Sara Wilcox, PhD, University of South Carolina
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
Pubblicazioni generali
- Baruth M, Wilcox S, Jake-Schoffman DE, Schlaff RA, Goldufsky TM. Effects of a Self-Directed Nutrition Intervention Among Adults With Chronic Health Conditions. Health Educ Behav. 2018 Feb;45(1):61-67. doi: 10.1177/1090198117709317. Epub 2017 Jun 3.
- Wilcox S, McClenaghan B, Sharpe PA, Baruth M, Hootman JM, Leith K, Dowda M. The steps to health randomized trial for arthritis: a self-directed exercise versus nutrition control program. Am J Prev Med. 2015 Jan;48(1):1-12. doi: 10.1016/j.amepre.2014.08.006. Epub 2014 Nov 6.
- Schoffman DE, Wilcox S, Baruth M. Association of body mass index with physical function and health-related quality of life in adults with arthritis. Arthritis. 2013;2013:190868. doi: 10.1155/2013/190868. Epub 2013 Dec 12.
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio
1 settembre 2009
Completamento primario (Effettivo)
1 luglio 2012
Completamento dello studio (Effettivo)
1 luglio 2012
Date di iscrizione allo studio
Primo inviato
17 maggio 2010
Primo inviato che soddisfa i criteri di controllo qualità
28 luglio 2010
Primo Inserito (Stima)
29 luglio 2010
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
28 aprile 2021
Ultimo aggiornamento inviato che soddisfa i criteri QC
26 aprile 2021
Ultimo verificato
1 aprile 2021
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- Pro00004658
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .