- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07621822
Telephone-Based Acceptance and Commitment Therapy for Young Adult Hazardous Drinkers
A Randomized Controlled Trial of Telephone-Based Acceptance and Commitment Therapy to Assist Young Adults With Hazardous or Harmful Alcohol Use to Quit Drinking
The goal of this clinical trial is to learn if telephone-based Acceptance and Commitment Therapy (ACT) works to help young adults with hazardous or harmful alcohol use quit drinking. It will also learn about the psychological effects of ACT on participants.
The main questions it aims to answer are:
- Does telephone-based ACT increase the number of participants who quit drinking, as confirmed by a urine test?
- Does telephone-based ACT help participants reduce their alcohol consumption and improve their psychological flexibility?
Researchers will compare telephone-based ACT to a telephone-based social support programme to see if ACT works to help young adults quit drinking.
Participants will:
- Receive telephone-based ACT or social support once a week for 6 weeks Complete questionnaires about their alcohol use and psychological flexibility.
- Keep a record of their daily alcohol consumption throughout the study using a standardised diary method.
- Provide a urine sample at the 6-month follow-up if they report having quit drinking
Studieoversikt
Status
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Ka Wai Katherine LAM, Doctor of Philosophy
- Telefonnummer: +852 27666420
- E-post: kw-katherine.lam@polyu.edu.hk
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- (1) aged 18-35 years
- (2) able to read Chinese and speak Cantonese
- (3) have AUDIT scores ≥ 8
Exclusion Criteria:
- (1) currently receiving other behavioural therapies for drinking
- (2) has serious mental illnesses, defined as a Kessler Psychological Distress Scale score ≥ 13
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Telephone-Based ACT Intervention
Telephone-based Acceptance and Commitment Therapy for participants
|
Participants in the intervention group will receive six weekly telephone sessions of ACT (45-60 min each) from interventionist.
|
|
Annen: Waitlist control with Telephone-Based Social Support
|
Participants in the control group will receive six weekly telephone sessions of social support (45 min each) from interventionist.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Biochemically-Validated Abstinence
Tidsramme: T4 (6 months after the end of the intervention)
|
Participants who self-report quitting drinking in the past 30 days are tested for ethyl glucuronide (a by-product of alcohol metabolism) via urine strips to confirm abstinence biochemically.
|
T4 (6 months after the end of the intervention)
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Self-Reported 30-Day Abstinence
Tidsramme: T0 (baseline), T1 (immediately after completion of the 6-week intervention), T2 (1 month after completing the intervention), T3 (3 months after completing the intervention), T4 (6 months after completing the intervention)
|
Reduction in alcohol consumption and self-reported 30-day abstinence will be recorded using TLFB.
Participants will be asked to report the number of drinks they have consumed within the past 30 days.
|
T0 (baseline), T1 (immediately after completion of the 6-week intervention), T2 (1 month after completing the intervention), T3 (3 months after completing the intervention), T4 (6 months after completing the intervention)
|
|
Reduction in Alcohol Consumption
Tidsramme: T1 (immediately after completion of the 6-week intervention), T2 (1 month after the intervention), T3 (3 months after the intervention), T4 (6 months after the intervention)
|
Defined as 50% or more reduction in average alcohol consumption per day compared to baseline, measured using the Timeline Follow-Back (TLFB) questionnaire.
|
T1 (immediately after completion of the 6-week intervention), T2 (1 month after the intervention), T3 (3 months after the intervention), T4 (6 months after the intervention)
|
|
Psychological Flexibility Index
Tidsramme: T0 (baseline), T1 (immediately after completion of the 6-week intervention), T2 (1 month after completing the intervention), T3 (3 months after completing the intervention), T4 (6 months after completing the intervention)
|
Personalised Psychological Flexibility Index(PPFI) will be used to measure psychological flexibility by 19 items rating on a 7-point scale.
Higher scores represent greater psychological flexibility.
It has been validated among Chinese college students
|
T0 (baseline), T1 (immediately after completion of the 6-week intervention), T2 (1 month after completing the intervention), T3 (3 months after completing the intervention), T4 (6 months after completing the intervention)
|
Samarbeidspartnere og etterforskere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- ACT Alcohol
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .