- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02335554
Internet Program for Workers With Subthreshold Depression (WorkDep)
Multimedia Internet-Based Program for Workers With Subthreshold Depression
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
The responsive mobile-web MoodHacker app was designed to: (a) educate users about depression; (b) educate users about the logistics and benefits of mood and activity monitoring; (c) promote daily mood and activity monitoring; (d) help users increase their positive activity engagement; (e) help users decrease negative thinking and increase positive thinking; and (f) promote daily practice of the skills taught.
Program content was adapted from the Coping with Depression group therapy course [18], enhanced with mindfulness-based [22] and other evidence-based positive psychology strategies [23-25]. Content for the application was refined based on input from experts in the field who had extensive experience working with adult employees at risk for depression. Additional program modifications were made based on data from individual interviews and iterative user testing with the population of interest during the formative and production phases of the project.
The MoodHacker user experience is structured around twelve learning objectives delivered through daily emails, in-app messaging, and in the "Articles & Videos" library. Daily emails (Figure 1) are sent to engage users in program content, provide sequenced guidance through the learning objectives in the articles and whiteboard-style videos, give tips for getting the most out of MoodHacker, and prompt the user to track their mood and activities daily. Users are encouraged to view the articles and videos as ordered, but viewing is not restricted, and users can view content according to their interest. The emails, articles and videos promote practice of the featured cognitive and behavioral skills outside the app experience.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- 18 years or older
- mild-to-moderate depressive symptoms as measured by the PHQ-9 (score of 10-19)
- not currently suicidal or meeting criteria for bipolar or schizo-affective disorder
- employed at least part-time
- English speaking
- access to a high-speed internet connection
Exclusion Criteria:
- younger than 18 years old
- severe depressive symptoms as measured by the PHQ-9 (score of 20+)
- currently suicidal or meeting criteria for bipolar or schizo-affective disorder
- employed less than part-time or unemployed
- not English speaking
- no access to a high-speed internet connection
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
---|---|
Sperimentale: MoodHacker
Participants in the treatment condition were emailed a link to the MoodHacker mobile-web app and instructed to use the program for the next six weeks.
Participants were asked to complete 2 follow-up assessments, 6 weeks and 10 weeks after baseline.
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Mobile-web app to educate users about depression and promote daily mood and positive activity monitoring.
Altri nomi:
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Comparatore attivo: Alternative Care
Alternative care participants were emailed and encouraged to browse links to vetted online information about depression.
Participants were asked to complete 2 follow-up assessments, 6 weeks and 10 weeks after baseline and were given access to the MoodHacker program after the 10-week assessment
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Online information about depression from government and other trusted sources to educate users about depression.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Depression symptoms as assessed by the Patient Health Questionnaire-9 (PHQ-9)
Lasso di tempo: 10 week follow-up
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Depressive symptomatology was assessed at each assessment point using the self-reported Patient Health Questionnaire-9 scale to assess the nine DSM-IV major depression symptoms.
The PHQ-9 is a self-report version of the Primary Care Evaluation of Mental Disorders (PRIME-MD) and has been shown to be a reliable and valid brief depression assessment tool.
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10 week follow-up
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Activation of positive self-care and life-choice behaviors
Lasso di tempo: 6-week posttest and 10-week follow-up
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How actively individuals are taking care of themselves, including making positive life choices, was expected to increase as a result of the intervention.
Behavioral activation was measured using the Behavioral Activation for Depression Scale Short Form (BADS).
This scale consists of 9 items.
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6-week posttest and 10-week follow-up
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Change in negative thinking
Lasso di tempo: 6-week posttest and 10-week follow-up
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Change in negative thinking was assessed using the Automatic Thoughts Questionnaire - Revised scale Short Form (ATQ-R-SF).
A 12-item adaptation of the ATQ-R instrument asked respondents to rate how many times over the past week they have had thoughts that are consistent with 12 negative self-statements.
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6-week posttest and 10-week follow-up
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Knowledge about depression
Lasso di tempo: 6-week posttest and 10-week follow-up
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Treatment participants were assessed for an increase in knowledge about depression.
The scale consisted of 14 multiple-choice items based on the 12 learning objectives addressed in the MoodHacker articles and videos.
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6-week posttest and 10-week follow-up
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Worker productivity as assessed by the Work Limitations Questionnaire
Lasso di tempo: 6-week posttest and 10-week follow-up
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Worker productivity was assessed using the Work Limitations Questionnaire (WLQ).
The WLQ Short Form consists of 10 items divided into four subscales measuring the degree to which a person was limited in their job's (1) time demands; (2) physical demands; (3) mental demands; and (4) output demands.
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6-week posttest and 10-week follow-up
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Worksite outcomes as assessed by the Workplace Outcomes Suite
Lasso di tempo: 6-week posttest and 10-week follow-up
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Worksite outcomes were also assessed using the Workplace Outcomes Suite (WOS).
The WOS is designed as an open-access instrument to facilitate empirical research on Employee Assistance Program (EAP) interventions.
The suite contains five 5-item scales that assess: absenteeism, presenteeism, work engagement, life satisfaction, and workplace distress.
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6-week posttest and 10-week follow-up
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User satisfaction as assessed by the System Usability Scale
Lasso di tempo: 6 week posttest
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Treatment participants completed the System Usability Scale, which is a quantitative measure of program ease of use.
The scale includes 10 items.
Users were asked to what degree they agreed or disagreed with program use and satisfaction statements on a 6-point scale (1=strongly disagree; 6=strongly agree).
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6 week posttest
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Collaboratori e investigatori
Investigatori
- Investigatore principale: Amy J Birney, MPH, MCHES, Oregon Center for Applied Science
Pubblicazioni e link utili
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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
- 81RR-2R
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 .