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Clinical Trials/NCT02253589
NCT02253589CompletedNot Applicable

Evaluation of Motivational Interviewing (MI) to Reduce Khat Use Among Somali Refugees in Kenya

University of Konstanz1 site in 1 country200 target enrollmentStarted: October 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
Time-Line-Follow-Back: Self-reported days with khat use and amount of khat use

Study Overview

Brief Summary

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.

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Healthy individuals

Exclusion Criteria

  • •Severe psychiatric disorders

Arms & Interventions

Waiting list

No Intervention

Participants will assessment only during study, same intervention after posttest

Intervention

Experimental

Participants assigned to this arm will receive the modified ASSIST-linked Brief Intervention

Intervention: modified ASSIST-linked Brief Intervention (Behavioral)

Outcomes

Primary Outcomes

Time-Line-Follow-Back: Self-reported days with khat use and amount of khat use

Time Frame: one month

Participants report in a calender for each day of the past month whether they used khat and how much of it.

Secondary Outcomes

  • Time-Line-Follow-Back: other substance use(One month)

Investigators

Sponsor
University of Konstanz
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Michael Odenwald

Researcher

University of Konstanz

Study Sites (1)

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