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3M Study - Maria Malmö Mobile Telephone Study

A Randomized Controlled Trial of Interactive Voice Response With and Without Personal Feedback in the Treatment of Adolescents With Substance Use Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01706380
Enrollment
73
Registered
2012-10-15
Start date
2012-10-31
Completion date
2014-04-30
Last updated
2021-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance Use Disorders

Keywords

Substance use disorders, Adolescents, Retention, Mobile telephone, Follow-up, Interactive voice response

Brief summary

The present study, in an out-patient setting for substance use treatment in adolescents, examines the effect on treatment retention of a mobile telephone follow-up technique (interactive voice response), with or without personal feedback. Subjects in treatment for substance use disorders will be followed by automated mobile telephone contact with questions about psychiatric symptoms and substance use, and the investigators hypothesize that this technique, including a personal feedback reporting back to the client whether his or her status is changing in one way or another, may increase the treatment retention, possibly by means of an intensified treatment contact.

Interventions

BEHAVIORALInteractive voice response with personal feedback

Personal feedback is given at the end of each automated telephone follow-up call, and reports back to the patient whether his och her symptom status is better, worse or equal, compared to the previous telephone call.

BEHAVIORALInteractive voice response without personal feedback

Control condition. Identical follow-up but without personal feedback.

Sponsors

Region Skane
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 25 Years
Healthy volunteers
No

Inclusion criteria

* Patient applying for substance use disorder treatment at out-patient facility Maria Malmö, Malmö, Sweden, who are less than 25 years old and who provide written informed consent to participate in the study.

Exclusion criteria

* Patients who do not provide written informed consent to the study, or whose psychiatric condition or language difficulties make it impossible for them to understand patient information and give informed consent to the study.

Design outcomes

Primary

MeasureTime frameDescription
Retention in substance use disorder treatment3 monthsDuration of retention in treatment and whether the client remains in treatment at 3 months or not.

Secondary

MeasureTime frameDescription
Improvement in substance use3 monthsDo patients in the intervention group improve more than in the control group, with respect to substance use (alcohol/drug use), during the duration of the interactive voice response intervention?
Improvements in psychiatric symptoms3 monthsDo patients in the intervention group improve more than in the control group, with respect to psychiatric symptoms, during the duration of the interactive voice response intervention?

Other

MeasureTime frame
Clinical course with respect to emergency visits12 months
Clinical course with respect to hospitalizations12 months
Clinical course with respect to repeated treatment episodes12 months

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026