- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00709501
Disseminating Effective Habits for Long-Term Weight Loss
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
Overweight and obesity are serious threats to public health. Over the last 20 years, the percentage of overweight and obese Americans, as well as the rate of diabetes, have grown tremendously (Cowie, Rust et al. 2006).
Few individuals are successful at long-term weight loss. Long-term weight loss is an elusive, yet sought after goal for many Americans (2000). Fewer than 5% of adults are successful in maintaining a 20 pound weight loss for at least 2 years (Klem, Wing et al. 1997). While medications can be effective, they produce only small amounts of weight loss, carry a significant cost and appear to be effective only while being taken (2000). Surgery is an effective option, though the procedure has tremendous costs and potential complications (2000). This points to the need for innovative and effective treatments that helps individuals over the longer-term.
Some, but not all, web-based treatments for weight loss have been shown to be effective. A recent study by Tate and colleagues showed that individuals who received counseling emails from a human or automated emails from a computer lost more weight than individuals who received neither(7.3 kg lost v. 4.9 kg and 2.6 kg, respectively) (Tate, Jackvony et al. 2006) (Tate, Jackvony et al. 2003). The feedback in the emails was based on diet and physical activity information that the individuals entered online. Dr. Harvey-Berino and colleagues has shown that social support delivered via the Internet can help weight loss efforts to the same degree as in person support (Harvey-Berino, Pintauro et al. 2004). Other studies have been mixed in their effects (Williamson, Walden et al. 2006) (Gold, Burke et al. 2007) (Wing, Tate et al. 2006), though there has generally been an effect from human feedback delivered via a computer. Other than the recent study by Tate and colleagues, no fully automated website has been effective at producing weight loss. It is our belief that fully automated systems are needed to meet the needs, in a cost-effective manner, of the 80 million overweight Americans who will need life-long help in losing weight and in maintaining their weight loss.
During an earlier phase of the study, 50 in-depth interviews were conducted with individuals who have been successful at losing weight and keeping it off. These individuals were asked specifically about which habits they use to maintain their weight loss, how these habits are implemented and how barriers to using these habits are overcome. These interviews were transcribed and the data entered into a website, to be used as part of the intervention to be tested in this clinical trial.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Pennsylvania
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Hershey, Pennsylvania, Stati Uniti, 17033
- Penn State College of Medicine General Clinical Research Center
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Age 21-65
- BMI 27-40 kg/m2
- Fluently speaks and reads English
- Access to the Internet at home or at work
- Valid email address
- Access to a scale for weekly weigh-ins
- Agree not to seek additional weight loss treatment
- Agree to come back regardless of amount of weight lost
- Participant in NCT00377208
Exclusion Criteria:
- Current, planned, or previous pregnancy within 12 months
- Planned or past weight loss surgery
- Recent weight loss of >= 15 lbs in the past 6 months
History of:
- Myocardial infarction
- Stroke
- Type 1 and Type 2 diabetes
- Unstable angina
- Congestive heart failure
- Inability to exercise due to severe arthritis or other musculoskeletal problems
- Cancer (except non-melanoma skin cancer)
- Evidence of severe cognitive impairment or major psychiatric illness
- Plans to move in the next 6 months
- Answering yes to any question on the Physical Activity Readiness Questionnaire (PAR-Q)
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Triplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
---|---|
Sperimentale: 1
Participants in the intervention condition are encouraged to access the Achieve Together website at least once each week. During each login, the following activities will occur:
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Comparison of weight change among those participants in the weight loss intervention (immediate access to the weight loss website) and those participants in the control group (delayed access to the weight loss website).
access to the Achieve Together website immediately (Arm 1) or delayed (Arm 2)
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Nessun intervento: 2
Participants in the control condition will have to wait 12 weeks before accessing the Achieve Together website.
These participants will be a given a log where they can document weekly weight measurements (this part did not happen).
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Body weight
Lasso di tempo: 3 months
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Weight will be measured using a calibrated, digital scale
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3 months
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Blood Pressure Control
Lasso di tempo: 3-Months
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3-Months
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Physical Activity, using the International Physical Activity Questionnaire
Lasso di tempo: 3 months
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Results are still being analyzed
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3 months
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Block 2005 FFQ for assessment of diet and physical activity
Lasso di tempo: 3 Months
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3 Months
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IWQOL-Lite, a validated, 31-item, self-report measure of obesity-specific
Lasso di tempo: 3 Months
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3 Months
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Christopher N Sciamanna, M.D., MPH, Penn State College of Medicine
Pubblicazioni e link utili
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
- 28160
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 .