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Testing Alcohol Interventions Among Job-seekers (TOPAS)

U

University Medicine Greifswald

Status and phase

Completed
Phase 2

Conditions

Hazardous Drinking

Treatments

Behavioral: Non-stage-tailored Intervention
Behavioral: Stage-tailored intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT01311245
FR2661/1-1 (Other Grant/Funding Number)
DM5-IESO03
FR2661/1-2 (Other Grant/Funding Number)
DM5-IESO05 (Registry Identifier)

Details and patient eligibility

About

The aim of the randomized controlled trial was to test two behavioral interventions among job-seekers with risky drinking. The interventions differed in their theoretical background: Intervention A was tailored to the stage of change, and Intervention B was non-stage-tailored. Over 12 months, job-seekers were pro-actively screened for risky drinking at three job-agencies. Job-seekers with risky drinking were asked to participate in the study. All three groups were assessed at baseline, and 3, 6 and 15 months later. The baseline assessment was self-administered using handheld computers. The follow-up assessments by interviews on the phone, primarily. Both intervention groups received individualized computer generated feedback letters at baseline and 3 months later.

Enrollment

1,243 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Job-seekers with risky drinking (AUDIT-C ≥ 4/5 [women/men] and AUDIT < 20)

Exclusion criteria

  • Job-seekers already asked to participate during an earlier visit at the job agency
  • Job-seekers not intending to talk to a job-agent/ without waiting time
  • Job-seekers physically or mentally not capable of participating in the study
  • Job-seekers with insufficient language/ reading skills
  • Job-seekers with more severe alcohol problems (AUDIT ≥ 20)
  • Job-seekers employed at the department conducting the study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

1,243 participants in 3 patient groups

Stage-tailored
Experimental group
Description:
At baseline and three months later
Treatment:
Behavioral: Stage-tailored intervention
Non-stage-tailored
Experimental group
Description:
At baseline and three months later
Treatment:
Behavioral: Non-stage-tailored Intervention
Control group
No Intervention group
Description:
Assessment only

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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