Psychotherapy, Therapeutic Alliance
Conditions
Keywords
Practice based research
Brief summary
This study evaluates a professional development program intended to improve the relationship or alliance between therapists and patients/clients who are receiving psychotherapy in the community. Half of the participating therapists will receive training to detect and improve alliance with new patients while half will not. The professional development training is expected to improve therapists effectiveness in identifying and correcting alliance tensions which will, in turn, improve therapeutic outcomes for patients/clients.
Detailed description
Psychotherapy is the treatment of choice for many mental disorders, yet there is a gap between research and practice. Research indicates that: the therapist-patient alliance is important to reduce patient symptoms, alliance tensions are detrimental to patients, and those therapists who identify and repair alliance tensions can improve patient outcomes. In this study we will use state of the art research to train community-based therapists in evidence-based interventions to identify and repair alliance tensions. Trained therapists and their patients will be compared to therapists who provide usual care to their patients. Improvement in therapists' skills in identifying and repairing alliance tensions and how this is associated with better patient mental health outcomes will be measured. Trained therapists will be interviewed to identify the best ways of improving the training and disseminating the findings to psychotherapists across Canada. Research to improve practicing therapists' ability to identify and repair therapeutic alliance tensions will result in better mental health outcomes for patients.
Interventions
OTHERProfessional development program
Professional development program consists of training including workshops and consultation sessions to enhance therapists ability to detect and repair alliance ruptures in active community based psychotherapy.
Sponsors
University of Ottawa
Canadian Institutes of Health Research (CIHR)
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Masking description
Participating therapists will be aware of their group (Asynchronous virtual training, synchronous virtual workshop training, no training control); however, their participating patient/clients will not know which experimental group their therapists belongs to.
Intervention model description
This will be a 2-arm, parallel, prospective, single-blind cluster RCT with 1-1 allocation comparing: (a) therapists who receive the professional development intervention to identify and repair alliance tensions at the study outset versus (b) therapists who receive the intervention after participation is complete (no training control). Therapists will be randomized to study condition and patients will be clustered within therapists. Randomization will control for: (a) the effect of therapist variables (age, gender, theoretical orientation, experience, differing initial skill level) on competence, therapeutic alliance, or patient outcomes; (b) potential biases caused by pre-treatment patient variables (symptom severity, co-morbidity, chronicity, psychoactive medications); and (c) treatment or study factors (e.g. frequency of sessions, time to complete the study sessions, treatment received after the study sessions). Patients will be blind to therapist study arm allocation.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Therapist Inclusion Criteria: * regulated health professional * in good standing with a Canadian provincial regulatory college * scope of practice includes psychotherapy * ability to add 3 or more new, English speaking clients to caseload over 6 to 9 months * ability to obtain timely permission to conduct research from therapist's employing institution or health group when applicable
Exclusion criteria
* none Patient/Client Inclusion Criteria: * 18 years of age or older * will participate in psychotherapy sessions in English * will see the study-affiliated therapist for a minimum of 6 sessions in the next 6 months
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mean tension resolution rating scale | 6 therapy sessions over 6 weeks up to 6 months depending on the frequency of therapy | The Rupture Resolution Rating System (3RS) is an observer-based measure to identify alliance tensions and resolution processes. Independent blind reliable trained judges will rate video recordings of 6 psychotherapy session recorded with participating clients. A mean tension score will be assigned per client which will be the average of the 6 session scores. score ranges from 1 (withdrawal/confrontation rupture(s) did not occur; not significant for the alliance) to 5 (withdrawal/confrontation rupture(s) occurred; significant for the alliance). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Generalized Anxiety Disorder 7-item scale (GAD-7) change from baseline | baseline and end of 6 therapy sessions, 6 weeks to 6 months depending on the frequency of therapy | Self-report measurement of severity of anxiety using the GAD-7 scale. A change in anxiety scores will be assess following 6 therapy session with data collected before therapy(baseline) and again after all 6 sessions of therapy have been completed. Scores range from 0 (low anxiety) to 27 (high anxiety) with scores over 10 being of clinical significance. |
| Patient Health Questionnaire 9-item scale (PHQ-9) change from baseline | baseline and end of 6 therapy sessions, 6 weeks to 6 months depending on the frequency of therapy | Self-report measurement of depression symptoms using the PHQ-9 scale. A change in depression symptom scores will be assess following 6 therapy session with data collected before therapy and again after all 6 sessions of therapy have been completed. Scores range from 0 (low) to 27 (high) with scores over 10 being of clinical significance. |
Countries
Canada
Contacts
PRINCIPAL_INVESTIGATORGiorgio Tasca, Ph.D.
University of Ottawa
Outcome results
None listed