- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03496350
Internet-delivered Cognitive Behavioural Therapy in Arabic for Anxiety and Depression
19. februar 2020 opdateret af: Gerhard Andersson, Linkoeping University
Culturally Adapted Transdiagnostic Internet-delivered Cognitive Behavioural Therapy in Arabic for Anxiety and Depression
The purpose of this study is to evaluate the efficacy of a culturally adapted internet-administrated cognitive behaviour therapy (ICBT) in Arabic for anxiety and depression
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The study will compare the effect of the intervention against a wait-list control.
The intervention tested is based on cognitive behavior therapy delivered over the internet via a secure treatment platform.
Participants in the study are recruited from the general public via social media.
The intervention is in Arabic.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
59
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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-
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Linköping, Sverige, 581 83
- Linköping University
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Be above 18 years of age
- Have symptoms of anxiety and/or depression
- Be able to read and write in Arabic
- Have access to computer or smartphone
Exclusion Criteria:
- Suicidal ideation
- Alcohol addiction
- Other major primary psychiatric disorder
- Ongoing psychological treatment
- Recent (during last 4 weeks) change in psychiatric medication
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Internet CBT
Internet-based cognitive behavioural therapy in Arabic with therapeutic guidance through email.
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Culturally adapted transdiagnostic internet-delivered CBT in Arabic
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Ingen indgriben: Wait-list
Wait-list control
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Change in Patient Health Questionnaire (PHQ-9)
Tidsramme: pre-treatment ,week 3, week 6, week 8 and 12 months post-treatment
|
The PHQ-9 is a nine-item self-report questionnaire that measures symptoms of depression.
It is scored from 0-27 with a higher score reflecting more severe symptoms.
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pre-treatment ,week 3, week 6, week 8 and 12 months post-treatment
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Change in Generalised Anxiety Disorder-7-item scale, (GAD-7)
Tidsramme: pre-treatment ,week 3, week 6, week 8 and 12 months post-treatment
|
The GAD-7 is a seven-item self-report questionnaire that measures symptoms of anxiety.
It is scored from 0-21 with a higher score reflecting more severe symptoms.
|
pre-treatment ,week 3, week 6, week 8 and 12 months post-treatment
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Alcohol Use Disorder Identification Test (AUDIT)
Tidsramme: pre-treatment, week 8
|
Measures alcohol consumption, drinking behaviors, and alcohol-related problems.
It is scored from 0-40 with higher scores reflecting more alcohol consumption, drinking behaviors, and alcohol-related problems.
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pre-treatment, week 8
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Insomnia Severity Index (ISI)
Tidsramme: pre-treatment, week 8
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Self-reported symptoms of insomnia.
It is scored from 0-28 with higher scores reflecting more symptoms of insomnia.
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pre-treatment, week 8
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Impact of Events Scale - Revised (IES-R)
Tidsramme: pre-treatment, week 8
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Self-reported symptoms of post-traumatic stress.
It is scored from 0-88 where higher scores reflect more symptoms.
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pre-treatment, week 8
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Perceived Stress Scale (PSS)
Tidsramme: pre-treatment, week 8
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Self-reported stress-related symptoms.
It is scored from 0-56 with higher scores reflecting more symtoms of perceived stress.
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pre-treatment, week 8
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"Brunnsviken Brief Quality of Life Scale" (BBQ)
Tidsramme: pre-treatment, week 8
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Self-reported quality of life.
The scale is scored from 0-96 with a higher score reflecting higher self-reported quality of life.
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pre-treatment, week 8
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
7. januar 2019
Primær færdiggørelse (Faktiske)
1. december 2019
Studieafslutning (Faktiske)
1. december 2019
Datoer for studieregistrering
Først indsendt
29. marts 2018
Først indsendt, der opfyldte QC-kriterier
5. april 2018
Først opslået (Faktiske)
12. april 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
20. februar 2020
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. februar 2020
Sidst verificeret
1. februar 2020
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- SAHA
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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