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Study of Effectiveness of Adding the Health Promotion and Rehabilitation for Treatment for Alcohol and Drug Abusers

Not Applicable
Completed
Conditions
Substance-Related Disorders
Chronic Disease
Malnutrition
Alcoholism
Smoking
Interventions
Behavioral: Health promotion activities
Registration Number
NCT01414907
Lead Sponsor
Skane University Hospital
Brief Summary

The purpose of this study is to evaluate the effect of adding the Health Promotion activities and rehabilitation to the usual alcohol and drug interventions on the outcome for alcohol and drug abusers compared to the usual intervention alone.

Detailed Description

Background: Alcohol and drug abuse are followed by tremendous physical, psychological and social problems as well as early death. Heavy smoking, poor nutrition, physical inactivity and chronic diseases (co-morbidity) are often part of these problems and illnesses.

There seems to be a large potential for a better outcome by including smoking cessation, physical training, diet and nutrition as well as co-morbidity in a multi-disciplinary setting - a potential not used yet. This Very Integrated Program (VIP) is inspired from the rehabilitation offered to patients with chronic diseases and surgical patients having a likewise unhealthy lifestyle and similar co-morbidity.

Aim: to evaluate the effect of adding the VIP program to the usual alcohol and drug intervention on the outcome for alcohol and drug abusers compared to the usual intervention alone.

The VIP project consists of 3 steps:

1. To map the health status and estimate the potential improvement for 400 alcohol and drug abusers

2. To pilot test the VIP program

3. To evaluate it compared to the daily routines for 260 alcohol and drug abusers with a poor health status in a randomised controlled trial.

Main outcome: Change from abuser to non-abuser. Secondary outcomes are health status; quality of life, use of health services, time return to work (or similar activity level), harm reduction, and cost-effectiveness.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
214
Inclusion Criteria
  • alcohol or drug dependency
Exclusion Criteria
  • withdrawal of informed consent
  • missing competence to give informed consent
  • pregnant or nursing women

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Health Promotion activitiesHealth promotion activities-
Primary Outcome Measures
NameTimeMethod
Change from abuser to non-abuser6 weeks, 3, 6, 9, 12 and 24 months
Secondary Outcome Measures
NameTimeMethod
Health status6 weeks, 3, 6, 9, 12 and 24 months
Quality of life6 weeks, 3,6,9,12 and 24 months
Harm reduction6 weeks, 3,6,9,12 and 24 months
Cost-effectiveness24 months

Trial Locations

Locations (1)

Addiction Center Malmo, Psychiatry Skane, Skane University Hospital

πŸ‡ΈπŸ‡ͺ

Malmo, Skane, Sweden

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