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Motivational Interviewing (MI) to Reduce Khat Use (MIkhat)

U

University of Konstanz

Status

Completed

Conditions

Khat Use Disorder

Treatments

Behavioral: modified ASSIST-linked Brief Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02253589
01DG13020

Details and patient eligibility

About

Healthy khat user with the intention to reduce or stop khat use will be randomly assigned to a one-session brief intervention or waiting list. Reductions in khat use will be measured from pre- to post-assessment which will be one month apart. After one month, the waiting list will receive the same intervention.

Full description

The leaves of the khat tree are traditionally chewed in some African and Arab countries. They contain the mild central stimulant cathinone. In recent years, the production, trade and use has dramatically increased and excessive patterns of use as well as a specific dependence syndrome have been described. So far, no experiences exist in psychological treatment of khat addiction.

In this study, we use a brief motivational intervention based on the WHO's ASSIST-linked Brief Intervention and Motivational Interviewing to support users who have the intention to reduce or stop their khat use. Khat users will be recruited in the community. Trained local staff will assess participant's khat and other substance use at study entry and one month later. Users will be assigned randomly to intervention or waiting list control groups. The intervention group will receive a single 20-minute brief intervention. The waiting list will receive the same intervention after the second assessment. After two months, a final assessment will be made in both groups.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy individuals

Exclusion criteria

Severe psychiatric disorders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 2 patient groups

Waiting list
No Intervention group
Description:
Participants will assessment only during study, same intervention after posttest
Intervention
Experimental group
Description:
Participants assigned to this arm will receive the modified ASSIST-linked Brief Intervention
Treatment:
Behavioral: modified ASSIST-linked Brief Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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