search
Back to results

PHAST: Physical Activity in Substitution Therapy (PHAST)

Primary Purpose

Substance-related Disorders

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Sport
Non-sport activities
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Substance-related Disorders focused on measuring craving

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patient at the Ambulanter Dienst Sucht or Janus clinics in Basel Town (BS); currently under substitution therapy

Exclusion Criteria:

Declared unfit to participate by clinic personnel due to physical disability or severe psychological disturbance or cognitive impairment

Sites / Locations

  • Department for Sport, Exercise and Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Sport Group

Control Group

Arm Description

Participants randomised to the exercise condition will receive 12 weeks of physical exercise training. Once they have been assigned to this group, they will be informed about the training programme and its content. Training will be carried out in groups (two groups of ten or four groups of five, depending on scheduling, sport preferences, available materials) to ensure that individual attention can be paid to each participant.

The control group will not receive any exercise training. In order to control, as far as possible, for the potentially therapeutic effects of extra contact time with investigators, and the potentially motivational elements of participation in an intervention, the C group will have equal contact time with an investigator and participate in a leisure program without physical activity component. This time will be filled with group mealtimes, games, films, painting, handcrafts, stretching or relaxation exercises.

Outcomes

Primary Outcome Measures

Craving measured by the Brief Substance Craving Scale (translated)
Craving will be measured by the Brief Substance Craving Scale (translated)
Secondary substance consumption assessed using the Time Line Follow Back method
This will be assessed using the Time Line Follow Back method

Secondary Outcome Measures

Depression assessed using the Allgemeine Depressionskala ( Depression Scale)
Depression will be assessed using the Allgemeine Depressionskala ( Depression Scale)
Self control measured using the Short Self Control Scale (translated)
This will be measured using the Short Self Control Scale (translated)
Subjective sleep measured using the Insomnia Severity Index (translated)
This will be measured using the Insomnia Severity Index (translated)
Physical activity level measured using the International Physical Activity Questionnaire
This will be measured using the International Physical Activity Questionnaire
Perceived Stress measured using the Perceived Stress Scale (translated)
Will be measured using the Perceived Stress Scale (translated)
Quality adjusted life years assessed using the Short Form (SF)36 questionnaire
This will be assessed using the Short Form (SF)36 questionnaire
Blood pressure measured using a digital sphygmomanometer
This will be measured using a digital sphygmomanometer
Lung function measured with a Spirobank Spirometer
Lung function will be measured with a Spirobank Spirometer
Hand grip strength assessed using a Hydraulic Hand Dynamometer.
This will be assessed using a Hydraulic Hand Dynamometer.

Full Information

First Posted
November 27, 2014
Last Updated
December 10, 2015
Sponsor
University Hospital, Basel, Switzerland
Collaborators
Psychiatric Hospital of the University of Basel
search

1. Study Identification

Unique Protocol Identification Number
NCT02309021
Brief Title
PHAST: Physical Activity in Substitution Therapy
Acronym
PHAST
Official Title
PHAST: Influence of Exercise Training on Substance Use, Substance Craving, Quality of Life, Mental Health, Sleep, and Physical Health in Patients Suffering From Opiate Dependence While Under Substitution Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
November 2014 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland
Collaborators
Psychiatric Hospital of the University of Basel

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim is to examine the effect of exercise (EX) training on individuals currently receiving ST - either opiate replacement therapy (ORT) or heroin-assisted treatment (HAT) - for their opiate dependence. Main outcome variables will be: cardiovascular fitness; consumption of substances (e.g. "street heroin", cocaine, cannabis, alcohol, cigarettes) other than prescribed ST or other prescribed medications; substance craving; blood pressure; lung function; resting pulse; social interaction; self-control capacity; objective and subjective sleep; cortisol levels; quality adjusted life years (QALYs); depression; mood. Covariates are current substitution dose and psychiatric diagnoses.
Detailed Description
The investigators aim is to carry out a randomized controlled trial comparing exercise training group and a control group of patients receiving substitution therapy (ST). The specific goals of the study are: To understand the exercise preferences, barriers to participation, motivation, experiences and attitudes regarding exercise training in patients under ST. To examine whether a 12-week exercise programme affects the mental health, subjective and objective sleep, quality of life, self-control capacity, substance craving, hair cortisol levels, secondary consumption, cardiovascular fitness, blood pressure, lung function, resting pulse, and social interaction in patients receiving ST. To compare the effects of the EX and control conditions on the above-mentioned outcome variables. To examine to what degree the covariates of heroin substitution dose and psychiatric comorbidities affect outcome variables. To explore to what extent objective variables (cardiovascular fitness, pulse, blood pressure, lung function, cortisol, objective sleep-EEG-parameters) and subjective-psychological dimensions (subjective sleep, social interaction, symptoms of depression and anxiety, self-control, substance craving) are interrelated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance-related Disorders
Keywords
craving

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sport Group
Arm Type
Other
Arm Description
Participants randomised to the exercise condition will receive 12 weeks of physical exercise training. Once they have been assigned to this group, they will be informed about the training programme and its content. Training will be carried out in groups (two groups of ten or four groups of five, depending on scheduling, sport preferences, available materials) to ensure that individual attention can be paid to each participant.
Arm Title
Control Group
Arm Type
Other
Arm Description
The control group will not receive any exercise training. In order to control, as far as possible, for the potentially therapeutic effects of extra contact time with investigators, and the potentially motivational elements of participation in an intervention, the C group will have equal contact time with an investigator and participate in a leisure program without physical activity component. This time will be filled with group mealtimes, games, films, painting, handcrafts, stretching or relaxation exercises.
Intervention Type
Other
Intervention Name(s)
Sport
Intervention Type
Other
Intervention Name(s)
Non-sport activities
Primary Outcome Measure Information:
Title
Craving measured by the Brief Substance Craving Scale (translated)
Description
Craving will be measured by the Brief Substance Craving Scale (translated)
Time Frame
6 months
Title
Secondary substance consumption assessed using the Time Line Follow Back method
Description
This will be assessed using the Time Line Follow Back method
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Depression assessed using the Allgemeine Depressionskala ( Depression Scale)
Description
Depression will be assessed using the Allgemeine Depressionskala ( Depression Scale)
Time Frame
6 months
Title
Self control measured using the Short Self Control Scale (translated)
Description
This will be measured using the Short Self Control Scale (translated)
Time Frame
6 months
Title
Subjective sleep measured using the Insomnia Severity Index (translated)
Description
This will be measured using the Insomnia Severity Index (translated)
Time Frame
6 months
Title
Physical activity level measured using the International Physical Activity Questionnaire
Description
This will be measured using the International Physical Activity Questionnaire
Time Frame
6 months
Title
Perceived Stress measured using the Perceived Stress Scale (translated)
Description
Will be measured using the Perceived Stress Scale (translated)
Time Frame
6 months
Title
Quality adjusted life years assessed using the Short Form (SF)36 questionnaire
Description
This will be assessed using the Short Form (SF)36 questionnaire
Time Frame
6 months
Title
Blood pressure measured using a digital sphygmomanometer
Description
This will be measured using a digital sphygmomanometer
Time Frame
6 months
Title
Lung function measured with a Spirobank Spirometer
Description
Lung function will be measured with a Spirobank Spirometer
Time Frame
6 months
Title
Hand grip strength assessed using a Hydraulic Hand Dynamometer.
Description
This will be assessed using a Hydraulic Hand Dynamometer.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient at the Ambulanter Dienst Sucht or Janus clinics in Basel Town (BS); currently under substitution therapy Exclusion Criteria: Declared unfit to participate by clinic personnel due to physical disability or severe psychological disturbance or cognitive impairment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Flora Colledge, PhD
Organizational Affiliation
Department for Sport, Exercise and Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department for Sport, Exercise and Health
City
Basel
ZIP/Postal Code
4052
Country
Switzerland

12. IPD Sharing Statement

Learn more about this trial

PHAST: Physical Activity in Substitution Therapy

We'll reach out to this number within 24 hrs