- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00818636
Expressive Writing for Co-Occurring Depression and Alcohol Misuse
***Please note that this study does not offer comprehensive treatment program for alcohol abuse or depression. Please do not contact the study staff if you are seeking psychological treatment. Further, this study is only enrolling people who are clients at Career and Recovery Resources, Inc., in Houston.
The hypothesis is that writing about feelings and thoughts will help people who are in group treatment feel less depressed and abuse alcohol less.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
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Texas
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Houston, Texas, Stati Uniti, 77004
- Career and Recovery Resources, Inc.
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
***Please note that this study does not offer comprehensive treatment program for alcohol abuse or depression. Please do not contact the study staff if you are seeking psychological treatment. Further, this study is only enrolling people who are clients at Career and Recovery Resources, Inc., in Houston.
Inclusion Criteria:
- Enrolled in group therapy program at Career and Recovery Resources, Inc.
- Must be at least 18.
- Willing and able to participate in the study through the one month follow up.
- Able to provide the contact information of at least two people who can generally locate their whereabouts.
- Speak English fluently.
Exclusion Criteria:
- Inability to read, write, speak English.
- History of bipolar or psychotic disorders.
- Severe medical, cognitive and /or psychiatric impairment that precludes cooperation with study protocol.
- Substance withdrawal symptoms requiring medical attention.
- Currently receiving other individual psychosocial therapy outside of C&R for substance abuse or other psychiatric conditions with the exception of AA, NA or CA.
- Impending incarceration or other factor that would create inability or unwillingness to participate in the 6 week long study period (e.g., halfway house or other aftercare program restrictions).
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
---|---|
Sperimentale: Expressive Writing
In addition to attending group therapy as usual, participants write about their feelings about an issue of their choosing three times during a two week period for at least 20 minutes each time.
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Participants in the expressive writing condition write about their feelings about an issue of their choosing three times, for at least 20 minutes each time, during a two week period.
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Comparatore attivo: Treatment as Usual
Participants attend group therapy as usual only.
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Participants in the expressive writing condition write about their feelings about an issue of their choosing three times, for at least 20 minutes each time, during a two week period.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
---|---|
Beck Depression Inventory, Second Edition
Lasso di tempo: Baseline, Post-writing (2 weeks post-baseline), and One Month Follow-Up (Six weeks post-baseline)
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Baseline, Post-writing (2 weeks post-baseline), and One Month Follow-Up (Six weeks post-baseline)
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Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
---|---|
Number of Alcoholic Drinks Consumed
Lasso di tempo: 30 days pre-baseline compared to 30 days post-intervention
|
30 days pre-baseline compared to 30 days post-intervention
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Carrie L Dodrill, Ph.D., The University of Texas Health Science Center at Houston- ** This contact information should not be used for counseling or informational purposes**
- Cattedra di studio: Angela L Stotts, Ph.D., The University of Texas Health Science Center at Houston- ** This contact information should not be used for counseling or informational purposes**
Pubblicazioni e link utili
Pubblicazioni generali
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
- 1R03AA016819-01A1 (Sovvenzione/contratto NIH degli Stati Uniti)
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 .