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Medication Free Treatment: Characteristics, Justification and Outcome

Medication Free Treatment: Characteristics, Justification and Outcome

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03499080
Enrollment
183
Registered
2018-04-17
Start date
2018-05-14
Completion date
2023-04-01
Last updated
2022-08-29

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

Conditions

Mental Illness

Keywords

Medication free treatment, mental illness, outcome

Brief summary

In 2015 the Norwegian government, after initiative from user organizations, decided to implement medication free inpatient treatment units. The goal is to secure real options to medication for psychiatric illness, and to gather experiences with medication free options. Freedom of choice is a main concern. The projects main aim is to study the outcome of medication free treatments of mental illness compared to treatment as usual, as well as characteristics of the treatment and the treatment population and why patients choose this treatment. Hereunder we aim to document who asks for these kinds of services and why, what kind of treatment they get, how they experience it, and how they respond to this kind of treatment. An important part will be to document whether the goal of increased freedom of choice between real treatment options is fulfilled. Research questions 1. Does medication free treatment differ from treatment as usual? Are there any unique characteristics of the patient group who asks for this kind of treatment? What kind of treatment do they receive during their stay? How do they experience this treatment in comparison to treatment as usual? How is this in relation to the goals about increased freedom of choice? Does use of medication change during and/or after medication free treatment? 2. Why do patients choose medication free treatment? What are their reasons? What experiences lead to this wish? 3. What is the outcome of medication free treatment compared to treatment as usual?

Detailed description

Background In 2015 the Norwegian government, after initiative from user organizations, decided to implement medication free inpatient treatment units. The goal is to secure real options to medication for psychiatric illness, and to gather experiences with medication free options. Freedom of choice is a main concern. (Aksjon for medisinfrie tilbud) The local unit under study DPS døgn Moenga at Akershus University Hospital has been given the assignment of developing a medication free treatment unit. This is an inpatient treatment unit for voluntary, planned treatment. High suicidal risk, severe acting out, active drug abuse etc. is excluded. The treatment program is 8 weeks long. Status of knowledge The project has been controversial, especially with reference to the status of knowledge. Critiques have stated that the knowledge base for treating serious psychiatric disorders without medication is lacking (Gundersen, 2016; Røssberg, 2016). Concerns are raised about whether it can be harmful (Røssberg, 2016), whether it is necessary (Røssberg, Andreassen, & Malt, 2016) and whether it creates unfortunate dividing lines within health care (Røssberg et al., 2016). National guidelines recommend considering/offering medication for bipolar disorders, deep depression and psychosis (Helsedirektoratet, 2009, 2012, 2013). On the other hand, the knowledge base for use of psychotropic drugs is also being questioned, especially regarding long term effects (Bentall, 2009; Forand & DeRubeis, 2013; Moncrieff, 2009; Sohler et al., 2016; Whitaker, 2010/2014 (no), 2016). Studies on medication are amongst others criticized for not taking withdrawal effect sufficiently into account (Bentall, 2009; Forand & DeRubeis, 2013; Moncrieff, 2009; Whitaker, 2010/2014 (no), 2016). A randomized controlled study by Wunderink, Nieboer, Wiersma, Sytema, and Nienhuis (2013) indicates a follow up period of at least 3 years is necessary to see the benefits of drug reduction regarding antipsychotics. Summing up, one can argue that generally, a considerable research base point to psychosocial treatment methods having an important place in the treatment of most psychiatric problems (Lambert, 2013; Wampold, 2001; Wampold & Imel, 2015). The more specific questions regarding pure psychosocial treatment for serious disorders and long term effects of psychotropic drugs are at least disputable, and probably under-researched. Research questions 1. Does medication free treatment differ from treatment as usual? Patient characteristics, treatment received, experience, medication use. 2. Why do patients choose medication free treatment? What are their reasons? What experiences lead to this wish? 3. What is the outcome of medication free treatment compared to treatment as usual? Hypotheses The treatment outcome of medication free treatment is not inferior to treatment as usual. Patients in medication free treatment will use less medication. Medication withdrawal may affect outcome in the short run. Project methodology The design of the study is a mixed methods, observational design within a naturalistic treatment setting using qualitative and quantitative methods to address the research questions. Moenga consist of two units, the medication free unit and a regular unit, which will be included for comparison. In addition we include a treatment unit on a different location for comparison; DPS Myrvegen. We aim for at least 200 n. One complication is that this autumn it was decided that the units at Moenga shall move and reorganize sometime during 2018. This entail change of location, possible reorganizing of personnel and that the comparison unit at Moenga is joined with another inpatient unit at the new location. This may cause disruptions that can affect our results. We will study possible effects of this in our data, and may exclude parts of the gathered data and prolong the inclusion period. We will collect survey data at start of treatment, weekly during treatment, at end of treatment (Work package 1), and at 6 months, 1 year, 2 years and 3 years follow up (work package 3). Register data will be collected 3 years back and 3 years follow up (work package 3). Patient interviews (work package 2) and personnel interviews (work package 4) are performed during spring 2018, the patient interviews near the end of the treatment stay. See measures for details. Plan for data analyses Quantitative and qualitative analyses will be done according to the research questions. We will seek to compare the medication free unit and treatment as usual. Calculating propensity scores in the observational part of the study will be considered, to balance comparison groups (Austin, 2011). Statistical power Exact power calculations are only possible in concrete, delimited statistical designs, and must necessarily be based on assumptions not always known before starting the study. In a design with 200 persons the total effect of one-way analysis of variance yield a statistical power of .80 for small to medium effect sizes. That is, the probability of detecting differences between groups will be .80 for effect sizes in the range .40 -.50. For pairwise comparisons between groups (with N=50), the probability of detecting effects in the range of Cohen's d \>=. 40 will be about .80. In Cohen's pragmatic system, effect sizes with such magnitudes represent a small to medium effect size. These estimations will also apply to change-scores between two points in time, given that the correlation between the two repeated measurements are r \>= .5. Study plan Data collection: Work package 1: Inclusion of patients for quantitative measurements starts April 2018 with a 12 months inclusion period. This may be prolonged if necessary. Work package 2: Patient interviews will be performed during spring 2018. Work package 3: Follow up measures and register data will be collected until spring 2022. Work package 4: Personnel interviews will be performed during spring 2018. Analysis Qualitative analyses will be performed within end of 2018. Quantitative analyses will start January 2019 Publishing Publishing of the results in scientific papers will take place mainly in 2019-2023. Articles 1. Medication free treatment: Does it differ from treatment as usual? This article will address research question 1 and include qualitative data, Collaborate, BMQ, Inspire, CSQ-8, WAI, treatment received, use of medication and background data. 2. Medication free treatment: Why? This article will address research question 2 (Why do patients choose medication free treatment) and include qualitative data. 3. Medication free treatment: Does it work? This article will address the research questions and will include the outcome measures OQ-45, AII, Quality of life, HoNOs, GAF, CGI, drug use, diagnoses and register data. We will also look for correlations between use of medication and outcome, and therefore include measures of medication use. Research group PhD Kristin S. Heiervang, head of the research group Quality and implementation in Mental Health Services at Akershus university hospital, is project manager (principal investigator) for the project. Anders S. Wenneberg, specialist in clinical psychology, is the leader of the inpatient treatment facility. Wenneberg is also the project manager of the Medication Free Treatment at Akershus University Hospital, Moenga. Ole André Solbakken is associate professor of clinical psychology and head of section at the Department of Psychology, University of Oslo. Odd Arne Tjersland is professor of clinical psychology at the Department of Psychology, University of Oslo. Jon T. Monsen is professor of clinical psychology at the Department of Psychology, University of Oslo. Allan Abbass is professor, psychiatrist, and founding Director of the Centre for Emotions and Health at Dalhousie University in Halifax, Canada. Kari Standal will be the PhD candidate. She is a psychologist at Akershus university hospital, specialized in adult treatment and psychotherapy (group treatment and affect consciousness). Jill Arild, board member of Mental Helse and leader of the action group for medication free treatment is user represantive in the project. Astrid Ringen Martinsen is a psychology student who will write her main thesis on the qualitative patient data. Ingrid Engeseth Brakstad is a psychology student who will write her main thesis on the qualitative personnel data.

Interventions

BEHAVIORALMedication free treatment

Inpatient unit dedicated to medication free treatment. This is an inpatient treatment unit for voluntary, planned treatment. The unit is staffed for a patient group that can be managed within a regime of open doors, voluntary treatment and low supervision. This means that high suicidal risk, severe acting out, active drug abuse etc. is excluded. They have an 8 week treatment program including Illness managment an recovery (IMR), Feedback informed treatment (FIT) and Affect consciousness treatment (ABT).

BEHAVIORALTreatment as usual Myrvegen

Inpatient unit on a different location from the others. Same Level of care. Different treatment program. Intermediate treatment duration (mainly 4-6 weeks).

BEHAVIORALTreatment as usual Åråsen

Unit colocated with the medication free unit. Similar treatment program. Short treatment duration (average 3 weeks).

Sponsors

University of Oslo
CollaboratorOTHER
University Hospital, Akershus
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Receiving planned treatment in the included treatment units * Are able to fill out questionnaires in Norwegian with minimal help / be interviewed in norwegian * Signed informed consent and willing to participate in the trial

Exclusion criteria

* Not able to fill out questionnaires or be interviewed in Norwegian. * Beds dedicated acute crisis and usercontrolled beds

Design outcomes

Primary

MeasureTime frameDescription
Outcome Questionnaire-45 (OQ-45)Filled out by patients at start of treatment, 1 time every week during the treatment program (typically 2 to 8 weeks), 1 time at end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsThis questionnaire was developed for tracking outpatients on a weekly basis. It measures symptom distress, interpersonal functioning and contentment with social role functioning, areas widely recognized as the essential ingredients of interest when assessing patient improvement. It is regarded suitable for patients with a wide range of diagnoses, sensitive to change over a short period of time, and brief and easy to administer (Lambert, Hansen, & Finch, 2001).

Secondary

MeasureTime frameDescription
Beliefs about medicines questionnaire (BMQ)Filled out by patients at start of treatment, end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsThe BMQ comprises two sections: the BMQ-Specific which assesses representations of medication prescribed for personal use and the BMQ-General which assesses beliefs about mcdicines in general. The pool of test items was derived from themes identified in published studies and from interviews with chronically ill patients. Principal Component Analysis (PCA) of the test items resulted in a logically coherent. 18 item, 4-factor structure which was stable across various illness groups. In this study we use the BMQ-Specific. The BMQ-Specific comprises two 5-item factors assessing beliefs about the necessity of prescribed medication (Specific-Necessity) and concerns about prescribed medication bascd on beliefs about the danger of dependence and long-term toxicity and the disruptive effects of medication (Specific-Concern).
Questionnaire on medication filled out by patientsat start of treatment, at 6 monts, 1 year, 2 years and 3 years.Questionnaire regarding psychotrophic medication based on questions from the project Bedre psykosebehandling
INSPIRE measure of staff support for personal recoveryFilled out by patients at start of treatment, end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsINSPIRE measure of staff support for personal recovery version 3 is included because the Recovery-tradition is a central part of the treatment program. Inspire has two subscales; Support and Relationship. The scale has demonstrated adequate psychometric properties (Williams et al., 2015).
CollaboRATEFilled out by patients at start of treatment, end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsCollaborate is a 3-item measure of shared decision making. CollaboRATE assesses three core SDM tasks: (1) explanation about health issues, (2) elicitation of patient preferences and (3) integration of patient preferences into decisions (Paul J. Barr et al., 2017). It has been found to have adequate psychometric properties in both simulated (Paul James Barr et al., 2014) and clinical (Paul J. Barr et al., 2017) settings.
The Client Satisfaction Questionnaire-8 (CSQ-8)Filled out by patients at start of treatment, end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsThe Client Satisfaction Questionnaire-8 (CSQ-8) is an eight item questionnaire for measuring patient's global satisfaction with services. It has been shown to correlate well with the longer version, CSQ-18, and has shown good psychometric qualities regarding internal consistency, attendance, remainer-terminator status and greater client-reported symptomreduction (Attkisson & Zwick, 1982)
Affect Integration Inventory 42 (AII-42)Filled out by patients at start of treatment, end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsAffect Integration Inventory 42 (AII-42) is a short version of AII, a medium-length (112 items) self-rated assessment instrument that endeavors to measure capacities for experience and expression of nine affect states. These are important parts of the construct affect integration, the capacity to utilize affects for personal adjustment. A recent study has found satisfactory reliability, sound internal structure, and associations with external criteria, indicating good convergent and discriminant validity (Solbakken, Rauk, Solem, Lødrup, & Monsen, 2017).
Life satisfaction questionFilled out by patients at start of treatment, end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsOne question regarding life satisfaction from the project from the MANSA instrument (Clausen et al., 2015).
Questions regarding whether they specifically sought medication free treatment and whyFilled out by patients at start of treatment.Questions regarding whether they specifically sought medication free treatment and why (self-developed)
Background dataFilled out by patients at start of treatment.Sosiodemographic data, contact with family and network, caregiving, juridical information, health service use, health history, drug use, physical health, health history (from the project Bedre psykosebehandling).
Treatment receivedFilled out by patients at end of treatment (typically week 2-8).A form regarding what kind of treatment they have received during the stay, and benefit (adapted from Sintef Unimed, 2002)
Use of drugsFilled out by patients at start of treatment, at 6 months, 1 year, 2 years and 3 yearsUse of drugs (questions from the project Bedre psykosebehandling).
The Working Alliance Inventory (WAI-SP)Filled out by patients at start of treatment, 1 time every week during the treatment program (typically 2 to 8 weeks), 1 time at end of treatment (typically at week 2-8) and at 6 months, 1 year, 2 years and 3 yearsThe WAI is one of the most widely used measures in research on working alliance and measures three aspects of the collaborative, purposive work in therapy: Bond, Task, and Goal. Research indicates that Bond, Task, and Goal represent the multidimensional construct working alliance is assumed to be (Horvath, 1994; ref. in Hersoug et al., 2009). WAI items are rated on a 7-point Likert-type scale ranging from 1 (never) to 7 (always), assessing the extent to which patient and therapist explicitly agree on the tasks and goals of therapy and the quality of the affective bond between them.
Health of the Nation Outcomes Scales (HoNOS)Filled out by clinician at start of treatment and end of treatment (typically week 2-8).Health of the Nation Outcomes Scales (HoNOS) was developed to routinely measure outcomes for adults with mental illness. It is regarded adequate for assessing outcomes for different groups on a range of mental health-related constructs, and appropriate for routinely monitoring outcomes (Pirkis et al., 2005).
Global assessment of functioning (GAF)Filled out by clinician at start of treatment and end of treatment (typically week 2-8).Global assessment of functioning (GAF) is one of the axes in the DSM diagnostic system from version III-R (Ullevål personlighetsprosjekt) until version 5. The multiaxial system was discarded in version 5 (Kress, Minton, Adamson, Paylo, & Pope, undated). From 1998 Statens helsetilsyn recommended all health institutions to use a minimum set of basic data (minste basis datasett) which included a split version of GAF called S-GAF (Ullevål personlighetsprosjekt). The patient is ranged on two scales from 0-100 regarding symptoms and functioning. The psychometric properties of GAF are disputed (Kress et al., undated), but the measure is short, widely applied and mandatory in hospitals and therefore we include it.
Scale on alcohol (AUS)Filled out by clinician at start of treatment and end of treatment (typically week 2-8).Scale on alcohol (AUS (Drake et al., 1990)
Scale on drugs (DUS)Filled out by clinician at start of treatment and end of treatment (typically week 2-8).Scale on drugs (Mueser et al., 1995))
DiagnosesFilled out by clinician at start of treatment and end of treatment (typically week 2-8).Diagnoses (including information on any diagnostic procedures used) (questions from the project Bedre psykosebehandling).
Patient interviewsThe interviews will be done close to the end of the treatment program (typically week 7).experience the treatment program, differences to other treatment they have been in and experience of freedom of choice regarding medication and other ways of coping. Interview guides will be developed by the phd candidate and a psychology student. The student will do pilot testing of the interview.
Register dataRegister data will be documented at baseline, and at 6 months, 1 year, 2 years and 3 years follow up.We will seek approval and consent to get data from national official registers on health and use of health services (Norwegian Patient Register, HELFO for primary health and social care, NAV).
Staff interviewsThe interviews are performed during spring 2018Interviews with staff on the medication free unit for exploring characteristics and differences to treatment as usual
Register data from the Medication Prescription RegisterCollected at 3 years before treatment start, 2 years before, 1 year before, 6 months post treatment, 1 year post treatment, 2 years post treatment and 3 years post treatmentUse of prescribed psychothropic medication
Questionnaire on medication filled out by clinicianat start of treatment and end of treatment (typically at 2-8 weeks)Questionnaire regarding psychotrophic medication based on questions from the project Bedre psykosebehandling
Help with medication filled out by patientat start of treatment, end of treatment (typically at 2-8 weeks) and at 6 months, 1 year, 2 years and 3 years.Help with medication: Questions developed in the project Bedre psykosebehandling about perceived quality of help and information regarding medication (Prosjekt Bedre psykosebehandling, n.d.).
The Clinical Global Impressions Scale (CGI)Filled out by clinician at start of treatment and end of treatment (typically week 2-8)The Clinical Global Impressions Scale (CGI) was developed for use in NIMH-sponsored clinical trials to provide a brief, stand-alone assessment of the clinician's view of the patient's global functioning prior to and after initiating a study medication (Guy, 1976; ref. in Busner & Targum, 2007) The CGI provides an overall clinician-determined summary measure that takes into account all available information, including a knowledge of the patient's history, psychosocial circumstances, symptoms, behavior, and the impact of the symptoms on the patient's ability to function. The CGI can track clinical progress across time and has been shown to correlate with longer, more tedious and time consuming rating instruments across a wide range of psychiatric diagnoses (Busner & Targum, 2007).

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026