AzTrials
AzTrials

AddictionNCT02510508

Group Version of CRAFT Compared to Self-Directed CRAFT Delivery and Non-intervention: a Three-armed RCT

A study testing Group CRAFT, Self-Directed CRAFT Delivery and Non-intervention in people with Addiction and Substance Use Disorder, run by IrisZorg at 6 sites in Netherlands.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
Search all trials

Trial summary

The aim of this study is to determine whether a group format Community Reinforcement and Family Training (CRAFT) and Self-Directed CRAFT Delivery are more effective than non-intervention in terms of Concerned Significant Others (CSO) well- being and cost- effectiveness. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Group CRAFT, Self-Directed CRAFT Delivery and Non-intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
29 participants
Where
6 sitesNetherlands
Study dates
Aug 2015to Feb 2017
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • CSO has concern about and having direct knowledge of alcohol- and/or drug problems of an IP, who is either a first degree relative, intimate partner or close friend.
  • Age at least 18 years (the CSO)
  • Reports that IP is not currently in addiction treatment (at IrisZorg and elsewhere) and has not received addiction treatment in the past 3 months
  • Reports that IP is treatment-refusing
  • Evidence (according CSO) that the IP meets criteria for SUDs according to The Structured Clinical Interview for DSM IV axis 1 Disorders (SCID-I)

Who cannot join

  • Does not demonstrate an adequate understanding of their participation, informed consent, and requirements of the protocol, or has insufficient reading abilities to comprehend the Dutch self-help book or does not agree to participate by refusing to sign an informed consent
  • CSO meets the DSM-IV criteria for any current SUD diagnosis, through clinical assessment by The Structured Clinical Interview for DSM IV axis 1 Disorders (SCID-I) and the Dutch version of the Mini- International Neuropsychiatric Interview ( M.I.N.I.)
  • Refuses to provide valid locator information, allow audiotaped sessions, and/or participate in follow-ups
  • Evidence that the IP had received treatment (other than detoxification) for alcohol or drug problems in the prior three months, was mandated by the courts to receive treatment, or was currently motivated to accept treatment
  • IP has a recent history of severe domestic violence
  • CSO is involved in a concomitant intervention to get the IP in treatment or to improve their own well-being
  • CSO fails to complete less than 4 Group CRAFT sessions

Trial locations and contacts

6 sites in 1 country.

6 sites in 1 country

Netherlands6 sites
  • IrisZorg

    Arnhem, Gelderland, 6800

  • IrisZorg

    Doetinchem, Gelderland, 7000

  • IrisZorg

    Ede, Gelderland, 6710

  • IrisZorg

    Nijmegen, Gelderland, 6500

  • IrisZorg

    Tiel, Gelderland, 4000

  • IrisZorg

    Zevenaar, Gelderland, 6900

Other trials in Netherlands

About this study

Official title: A Group Version of Community Reinforcement and Family Training (CRAFT) Compared to Self-Directed CRAFT Delivery and Non-intervention: a Three-armed Randomized Clinical Trial

The aim of this study is to determine whether a group format Community Reinforcement and Family Training (CRAFT) and Self-Directed CRAFT Delivery are more effective than non-intervention in terms of Concerned Significant Others (CSO) well- being and cost- effectiveness.

Read the detailed description

The aim of this study is to determine the applicability and effectiveness of (a) CRAFT group format in conjunction with the CRAFT self-help book and (b) a CRAFT self-help book (self-directed CRAFT delivery condition), compared to (c) non-intervention (control). The primary aim is increase CSO well- being and reduce CSO health complaints. CSOs will be assessed at baseline (T0), 2 months (end of intervention) (T1), 3 months- (T2), and 6 months follow-up (T3), independently of the assigned condition. Secondary outcomes will encompass cost-effectiveness of both CRAFT interventions. Also, we measure IP engagement and IPs' substance use.

Since the negative consequences of substance abuse are not limited to alcohol- and drug users themselves, it also affects the lives of family members and close friends (CSOs). This study focusses on CSOs to improve their lives. Recruitment will take place in the Netherlands (nation- wide). Assessment and the CRAFT group intervention will be conducted at six different locations (Arnhem, Doetinchem, Ede, Nijmegen, Tiel and Zevenaar, all in the province of Gelderland) in the Netherlands. Participants will be recruited via advertisements on the Internet, social media, websites of IrisZorg (centre for addiction care and sheltered housing ), and subsequently, in local newspapers and flyers located in emergency rooms, general practitioners, family practice clinics, and mental health based treatment agencies.

To obtain information about the presence of psychiatric disorders of the CSOs, a Dutch version of the Mini-International Neuropsychiatric Interview (M.I.N.I.) will be used. After initial assessment, a randomization procedure will be conducted by an independent researcher, who is affiliated to the Erasmus Medical Center, Rotterdam, the Netherlands. CSOs will be informed about the allocation of conditions within 1 week, after initial admission. Several outcome measures will be used in this study. The following will be measured:

  1. CSO well- being (including physical and psychological health and complaints, quality of life, quality of the relationship, self- efficacy and social support);
  2. cost-effectiveness of both CRAFT and Self- Directed Delivery compared to non- intervention.
  3. IP engagement and IP substance use.

Using the primary outcome, CSO well-being, a priori power analysis is completed. Means and standard deviations for CSO well-being, measured with the Beck Depression Inventory (BDI), for Group CRAFT were used (Miller et al., 1999). An effect size was calculated (f = 0.22). The power analysis, conducted with the online program called G-power, indicated that a total sample size of 69 CSOs is needed to achieve a power of 95% for detecting a medium effect size when using the p = 0.05 criterion of statistical significance. These numbers are based on an ANOVA with a within-between subject design. Based on the pilot study of Kirby et al. (1999), 23% drop out after 3- and 6- month follow-up is taken into account. This means that, including the 23% drop-out-rate and based on the sample size of 69, an N of 85 is needed after 3 months and that a total N of 105 is needed to complete all assessments. Summarized, to be able to have at least 69 assessments completed at 6- month follow- up, a total sample size of 105 CSOs is required; with an estimated total drop-out rate of 34%.

Being tested
Group CRAFT, Self-Directed CRAFT Delivery, Non-intervention
Keywords
addiction, substance abuse, alcohol, drugs, community reinforcement, family treatment, randomized control trial
Medical subject headings
Behavior, Addictive, Substance-Related Disorders, Alcoholism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Group CRAFTBehavioural

    CSOs will receive seven weekly 90 min sessions of CRAFT + Self-Directed CRAFT Delivery

  • Self-Directed CRAFT DeliveryBehavioural

    Also called CRAFT self-help book condition

    CRAFT self-help book (Self Directed CRAFT Delivery)

  • Non-interventionOther

    Also called Waitinglist condition

    Non-intervention

Study groups in NCT02510508
Study groupRoleWhat they receive
Group CRAFTExperimentalAll CSO's who are allocated to CRAFT group condition will be offered seven sessions of a CRAFT Group format. Each group will meet for 90 minutes weekly and will be completed within 2 months. The group content is based on the CRAFT techniques described by a training manual written by Roozen, Smith and Meyers (2015). Furthermore the CSOs in this condition will also receive a Dutch version of the CRAFT self-help book (Self Directed CRAFT Delivery), "Get your loved one sober: Alternatives to nagging, pleading and threatening" (Meyers \& Wolfe, 2012). Groups will engage in a combination of didactic teaching, role-play of new communication styles and discuss their experiences utilizing CRAFT skills.
Receives: Behavioral: Group CRAFT; Other: Non-intervention
Self-Directed CRAFT DeliveryActive comparatorCSO's allocated to the Self- Directed CRAFT Delivery will receive the Dutch version of the CRAFT self-help book, "Get your loved one sober: Alternatives to nagging, pleading and threatening" (Meyers \& Wolfe, 2012). The book helps CSO's how to utilize the CRAFT model in their daily lives. It includes guidelines for responding to IP behavior, improving positive communication skills, improving the CSO's own well-being and explains how to engage the IP into treatment.
Receives: Behavioral: Self-Directed CRAFT Delivery; Other: Non-intervention
Non-interventionNo interventionParticipants assigned to the non-intervention condition will be placed on a Group CRAFT waiting list.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Concerned Significant Other (CSO) well-being (physical and psychological)

    Measured by the following tests:Measurement of the Addictions for Triage and Evaluation (MATE), Depression Anxiety Scales (DASS-21), Maudsley Addiction Profile (MAP), Research and Development- 36 (RAND- 36), Trimbos/iMTA questionnaire for Costs Associated with Psychiatric Illness (TicP) and EuroQol- 5D.

    Measured: 4 months after the initiation of the intervention

Secondary outcomes (4)
  1. CSO quality of life

    Measured by the following tests: CRA- Happiness Scale (CRA-HS) and WHOQol- Bref

    Measured: 4 months after the initiation of the intervention

  2. CSO quality of the relationship

    Measured by the following tests: CRA Relationship Happiness Scale (CRA-RHS), Agression Questionnaire (AQ) and Experiences in Close Relationships Scale- short form (ECR)

    Measured: 4 months after the initiation of the intervention

  3. Other CSO reported psychological measures

    Measured by the following tests: General Self-Efficacy Scale (GSES) and Social Support Inventory (SSI).

    Measured: 4 months after the initiation of the intervention

  4. Cost-effectiveness of group CRAFT and Self-Directed CRAFT Delivery compared to non-intervention condition

    Measured by: TiC-P; EuroQol- 5D and RAND-36

    Measured: 4 months after the initiation of the intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jul 2015 (estimated)
  2. Study startAug 2015
  3. Primary completionOct 2016
  4. Study completionFeb 2017

Why it stopped: Not enough participants were included

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
29 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02510508
Sponsor's protocol ID
NL48307.028.14
Status last verified
Aug 2017
First submitted
16 Jul 2015
Last updated
21 Aug 2017
Results posted
No
Data monitoring committee
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Group CRAFT, Self-Directed CRAFT Delivery and Non-intervention in people with Addiction and Substance Use Disorder, run by IrisZorg at 6 sites in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 21 Aug 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Not enough participants were included). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Concerned Significant Other (CSO) well-being (physical and psychological) (time frame: 4 months after the initiation of the intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Aug 2017; AzTrials last refreshed its copy on 31 Oct 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in