ClinicalTrials.gg
Not yet recruitingNCT07621822Updated Aug 17, 2026

Telephone-Based Acceptance and Commitment Therapy for Young Adult Hazardous Drinkers

An interventional study of Telephone-Based Acceptance and Commitment Therapy (ACT) and Waitlist control with Telephone-Based Social Support in Hazardous Drinking and Harmful Alcohol Use, sponsored by The Hong Kong Polytechnic University. Not yet recruiting. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-08-17.

Sponsored by The Hong Kong Polytechnic University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
288
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

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:

  1. Does telephone-based ACT increase the number of participants who quit drinking, as confirmed by a urine test?
  2. 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:

  1. Receive telephone-based ACT or social support once a week for 6 weeks Complete questionnaires about their alcohol use and psychological flexibility.
  2. Keep a record of their daily alcohol consumption throughout the study using a standardised diary method.
  3. Provide a urine sample at the 6-month follow-up if they report having quit drinking
02

Conditions studied

  • Hazardous Drinking
  • Harmful Alcohol Use

Browse trials for

Keywords

  • Acceptance and Commitment Therapy
  • Telephone-based intervention
  • Alcohol use
  • Psychological flexibility
  • Randomized controlled trial
03

In context

Alcohol Drinking

701 studies on the registry are indexed under Alcohol Drinking; 133 are open to participants now.

This study's planned enrollment of 288 is above the median of 122 across 607 interventional studies indexed under Alcohol Drinking.

Browse Alcohol Drinking studies →

Lead sponsor

The Hong Kong Polytechnic University is the lead sponsor of 679 studies on the registry; 257 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • (1) aged 18-35 years
  • (2) able to read Chinese and speak Cantonese
  • (3) have AUDIT scores ≥ 8

Exclusion criteria

Exclusion Criteria:

  • (1) currently receiving other behavioural therapies for drinking
  • (2) has serious mental illnesses, defined as a Kessler Psychological Distress Scale score ≥ 13
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
288 participants (estimated)

Study arms

  • Experimental
    Telephone-Based ACT Intervention

    Telephone-based Acceptance and Commitment Therapy for participants

    Behavioral: Telephone-Based Acceptance and Commitment Therapy (ACT)

  • Other
    Waitlist control with Telephone-Based Social Support

    Waitlist control with Telephone-Based Social Support

    Behavioral: Waitlist control with Telephone-Based Social Support

Interventions

  • BehavioralTelephone-Based Acceptance and Commitment Therapy (ACT)

    Participants in the intervention group will receive six weekly telephone sessions of ACT (45-60 min each) from interventionist.

  • BehavioralWaitlist 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.

06

What researchers measure

Primary outcomes

  1. Biochemically-Validated Abstinence

    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.

    Time frame: T4 (6 months after the end of the intervention)

Secondary outcomes

  1. Self-Reported 30-Day Abstinence

    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.

    Time frame: 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)

  2. Reduction in Alcohol Consumption

    Defined as 50% or more reduction in average alcohol consumption per day compared to baseline, measured using the Timeline Follow-Back (TLFB) questionnaire.

    Time frame: 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)

  3. Psychological Flexibility Index

    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

    Time frame: 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)

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Aug 2026; primary completion for Jul 2029, 35 months later.

Of 328 non-industry interventional studies with no phase under Alcohol Drinking, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 45. This study's planned 35 months is above that.

Counting every sponsor, half of 336 studies reached it within 24 months; a quarter within 10 and three quarters within 45.

How these figures are worked out, and which studies are left out of them.

Registered
May 26, 2026
First posted
Jun 2, 2026
StartEst.
Aug 1, 2026
Primary completionEst.
Jul 31, 2029
CompletionEst.
Jul 31, 2029
Last update
Aug 17, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07621822
Responsible party
Dr Katherine Lam (Assistant Professor, The Hong Kong Polytechnic University) — Principal investigator
First posted
Jun 2, 2026
Start date
Aug 1, 2026 (estimated)
Primary completion
Jul 31, 2029 (estimated)
Completion
Jul 31, 2029 (estimated)
Last update
Aug 17, 2026

Study contacts

Ka Wai Katherine LAM, Doctor of Philosophy
Contact
kw-katherine.lam@polyu.edu.hk
+852 27666420

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion