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

S

Skane University Hospital

Status

Completed

Conditions

Alcoholism
Chronic Disease
Malnutrition
Substance-Related Disorders
Smoking

Treatments

Behavioral: Health promotion activities

Study type

Interventional

Funder types

Other

Identifiers

NCT01414907
VIP-LU-2011

Details and patient eligibility

About

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.

Full 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.

Enrollment

214 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • alcohol or drug dependency

Exclusion criteria

  • withdrawal of informed consent
  • missing competence to give informed consent
  • pregnant or nursing women

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

214 participants in 2 patient groups

Health Promotion activities
Active Comparator group
Treatment:
Behavioral: Health promotion activities
No Intervention
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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