- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02765542
Developing Accessible mHealth Programs for Depression Management in Bolivia
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
All patients will receive a weekly 10-15 minute automated phone call to their cell phone for disease assessment and self-care support for up to 12 weeks. During enrollment, the research team will explain how to use the automated phone system. During patients' automated calls, they will be asked questions about their self-care relevant to their diagnosis, symptoms of depression, and medication adherence (if patients are prescribed an anti-depressant). Based on the patient's self-report, they will receive targeted suggestions for how to improve their self-management. At the end of each automated call, patients will hear the phone number of their clinic, which they can call for a health problem or to disenroll from the program. At the time of recruitment, if possible, an initial automated call will be sent to the patient's phone so that they can learn what to expect and have the chance to ask questions of the research associate who will be present.
In the event that the patient reports a health or self-care problem during their call (i.e., the patient reports rarely or never taking their medication), a report will automatically be generated and sent by email to the research team plus the patient's designated clinician so that follow-up can take place. The secure email address will be verified with each clinician, and be password protected.
The intervention will last up to 12 weeks, after which the patient will have a follow-up meeting with the research team and will complete a survey about the program. All follow-ups will take place either in person or over the phone.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
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La Paz, Bolivia
- El Servicio Departmental de Salud (SEDES) affiliated clinics
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- 21-80 years of age
- PHQ-8 score of 10 or higher
Exclusion Criteria:
- Have diagnoses indicating a six-month life expectancy
- Prior inpatient psychiatric treatment
- Patients with probable bipolar disorder or cognitive impairment as indicated on validated screeners
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Hälsovårdsforskning
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: Automated phone calls
Automated disease assessment & self-care support phone calls for up to 12 weeks.
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Automated disease assessment & self-care support phone calls for up to 12 weeks.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
---|---|
Change from baseline on depressive symptoms at 12 weeks (PHQ-8 Scores)
Tidsram: Baseline and 12 week post-intervention follow-up
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Baseline and 12 week post-intervention follow-up
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Sekundära resultatmått
Resultatmått |
Tidsram |
---|---|
Change from baseline on self-care behaviors at 12 weeks (self-care behavior questionnaire)
Tidsram: Baseline and 12 week post-intervention follow-up
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Baseline and 12 week post-intervention follow-up
|
Evaluate program feasibility (telephone call completion rates)
Tidsram: 12 week post-intervention follow-up
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12 week post-intervention follow-up
|
Patient satisfaction (satisfaction questionnaire)
Tidsram: 12 week Post-intervention follow-up
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12 week Post-intervention follow-up
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Patient qualitative feedback (qualitative questionnaire)
Tidsram: 12 week Post-intervention follow-up
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12 week Post-intervention follow-up
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: John D Piette, PhD, University of Michigan
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- HUM00087937
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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