- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04243018
Feasibility Trial of an Acceptance and Commitment Therapy Intervention for Individuals Experiencing Homelessness
Feasibility Pilot Randomised Control Trial for Brief Acceptance and Commitment Therapy (ACT) Intervention for Adults Experiencing Homelessness to Enhance Well-Being and Mitigate the Deleterious Effects of Shame and Self-Stigma
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
On average homeless persons have higher rates of childhood and adult adversity, challenging behaviour, substance and alcohol misuse, poor educational, occupational achievement, co-morbid physical and mental illness. In mental health, services delivered on the basis of address can struggle to mount a satisfactory response to the needs of homeless persons. Many homeless persons rely on emergency department visits or inpatient hospitalizations for health care. When admitted to hospital, they have longer stays with higher costs. With the rates of homelessness increasing in both national and international contexts coupled with the several barriers to accessing mainstream health services, the development of brief, cost-effective interventions, that address comorbidity of various mental illnesses and substance abuse is necessary.
In addition, individuals who have experienced homelessness can have their growth and development curtailed by applying a punitive, shame based, and defeatist perspectives to their own goals and values in life. Direct acts or discrimination, as well as diminished opportunities offered to people experiencing homelessness, can be understood as a manifestation of public stigma. Labelling someone as "homeless" or an "addict" tends to activate common stereotypes such as thinking that the person is likely to be unreliable, deceitful, or weak, among other stereotypes. This often leads to some sort of social sanction or devaluation, reducing the probability of the person being hired, or being trusted as a parent, friend, or lover.
People who identify with a stigmatised group often internalise the stereotypes associated with that group. In addition, the effects of enacted stigma, the emotional and cognitive barriers erected by the individual experiencing homelessness in response to perceived or experienced stigma, can also serve to obstruct access to opportunities. The person may self-identify as a loser, being damaged goods, or always hurting others. Attachment to these self-conceptions entails giving up on important and valued life directions. These are manifestations of self-stigma. Studies of individuals with serious mental illness and co-occurring disorders have shown that self-stigma is associated with delays in treatment seeking or avoidance of treatment, diminished self-esteem/self-efficacy, increased mental health symptoms, and lower quality of life. Therefore, it is imperative that interventions actively address and aim to mitigate the deleterious effects of shame and self-stigma.
Assertive Community Treatment and case-management interventions have been proven moderately effective in improving mental and physical health outcomes for homeless populations, however, the resources and expertise required to run such interventions are; unavailable to most sectors and communities, time consuming and normally used on an individual case basis, leaving large portions of this population untreated. Research into brief psychological interventions with the homeless population has revealed promising effects, however, these interventions often target specific sub-populations, chose to focus on one aspect of recovery such as substance abuse and do not address comorbidity of illness.
The Acceptance and Commitment Therapy(ACT) model is compatible with conceptualisations of recovery from severe mental illness (defined as "living a satisfying, hopeful and contributing life even with limitations caused by the illness"; and "having a sense of purpose and direction"). From an ACT perspective 'addictive-', 'depressive-', 'anxiety'- and "stress-' behaviours might share the same function; and those with high levels of comorbidity, such as the homeless population might therefore be treated using an ACT.
The focus on specific cognitive behavioural processes of mindfulness, acceptance, distancing, and values-based action makes ACT interventions typically brief and have been proven to be effective after a single session and mediation studies suggest that the positive clinical effects of ACT are achieved by changing these targeted psychological processes.
A two-arm feasibility pilot randomised control trial will be conducted to investigate differences in the proposed outcome variables between participants assigned to a group-based ACT intervention and those assigned to peer support group. A process level investigation will also be used to investigate the feasibility of conducting a full scale RCT with the population.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Dublin, Ireland, D8
- Merchants Quay Ireland
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Dublin, Ireland
- Focus Ireland
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Dublin, Ireland
- Peter McVerry Trust
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Service Users: Individuals who are currently experiencing or have experienced homelessness in the past year.
Over 18 and under 65.
- Service Providers: Have been working with homeless services for over a year, in close contact with service users. Over 18 and under 65.
Exclusion Criteria:
- Participants with severe mental health issues- Currently experiencing suicidal ideation or active psychosis
- Participants with serious cognitive impairments
- Participants with below conversational level proficiency in English
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Acceptance and Commitment Therapy
Acceptance and Commitment Therapy Intervention to improve well-being and reduce the negative effects of shame and self-stigma in a population of adults experiencing homelessness.This will involve participating in two sessions, lasting two and a half hours each, over a period of two weeks.
Well-being will be promoted in each session by targeting core processes of the ACT model including acceptance, cognitive defusion, mindfulness, flexible perspective taking, values clarification and committed action.
In addition participants will be provided with an acceptance and commitment training workbook.
The workbook will foster core processes of the ACT model through psycho-education, daily exercises, tips and tools.
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The intervention presents, a mixture of instruction, discussion, and the use of metaphor and experiential activities designed to sensitise participants to the effects of self-stigma and shame on how they live their lives.
This training condition provides instruction and experiences that train participants to notice, and then to override, the very human tendency to categorise and then avoid aversive thoughts and feelings and the people and situations that evoke them.
The acceptance and commitment training condition will cover the following topics: (a) introduction to enacted and self-stigma (b) cognitive defusion/behavioural flexibility (c) acceptance vs. avoidance and control of emotions and thoughts and (d) values and committed action.
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Active Comparator: Peer Support Group
This peer support group will involve discussing themes around experiencing homelessness, shame and stigma and will be facilitated by an experienced peer support group leader.This will involve participating in two sessions, lasting two hours each, over a period of two weeks.
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The peer support group will allow participants to share and discuss experiences related to their experiences of homelessness, shame and stigma.
The group will be facilitated by an expert in facilitating peer support groups with marginalised populations.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Internalised Shame Scale (Cook, 1996)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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30-item measure that assess shame proneness and internalised shame.
It also contains a 6-item self-esteem scale.Respondents must rate each self-statement on a Likert-type scale from 0 to 4, with each number anchored to the words, "Never", "Seldom", "Sometimes", "Often", and "Almost Always", respectively.
Higher scores indicate more problematic levels of internalised shame.
Higher scores on the self-esteem sub-scale indicate positive self-esteem.
Scores of the sub-scales are summed to provide a total score for internalised shame.
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Self-Stigma Scale- Short (Mak & Cheung, 2010)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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a 9-item measure that is conceptualised along three psychological dimensions (viz., self-stigmatising cognition, affect, and behaviour), and corresponds to cognitive-behaviour theory.Each item asks the respondents to rate their agreement on a 4-point Likert scale from 1 (strongly disagree) to 4 (strongly agree).
Higher score on the SSS-S represents a higher level of self-stigma.
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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World Health Organisation- Five Well-Being Index (WHO, 1998)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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5-item short self-reported measure of current mental well-being.
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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CompACT Scale (Francis, Dawson, & Moghaddam, 2016)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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23-item measure assessing Acceptance and Commitment Therapy specific outcomes, psychological flexibility, valued action, openness to experience, and behavioural awareness.
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Identifying Levels of Treatment Engagement
Time Frame: 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Semi-structured interviews will also be conducted with a service user from each group and with service providers, this done in order to assess treatment engagement and also inform a process level investigation.
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1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Therapist Fidelity and Adherence
Time Frame: 3-months post-baseline (follow-up)
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Treatment fidelity will be assessed post-intervention by 2 independent reviewers (members of the Contextual Behavioural Sciences lab in UCD).
This will involve reviewers listening to the same 10-minute recording from each session and listing the ACT processes they can identify within the 10-minute recording.
With the aim of achieving a minimum of 70% consensus between reviewers.
Therapists will also have to write down what exercises were used to teach each of the ACT processes post-intervention for each session and will be assessed by the independent reviewers to assess protocol adherence; were all of the ACT processes taught and were the exercises in the protocol used.
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3-months post-baseline (follow-up)
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Study Feasibility Interviews
Time Frame: 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Service users will be asked about the practicalities of participating the study (e.g.
experience of answering questionnaires), experiences of the group, how the intervention has impacted the environment in the shelter, what they found most beneficial, recommendations for improvements, and engagement with intervention and the use of skills learned.Service provider interviews will explore, feasibility of the intervention, resource management, staff-researcher communication and the intervention.
Results from these interviews, therapist adherence and fidelity, and analysis of retention and attrition will be the process-based outcomes from the study.
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1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Participant Retention and Attrition
Time Frame: Post-completion of data collection an average of one-year
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Percentage of participants retained at 8-week follow-up.
Percentage of participants who attended each session and data collection point
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Post-completion of data collection an average of one-year
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Client Satisfaction Questionnaire-8 (CSQ-8; Attkisson, Hargreaves & Nguyen, 1978)
Time Frame: 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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8-item self-report statement of satisfaction with health and human services.
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1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Cognitive Fusion Questionnaire (Gillanders et al., 2014)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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seven items rated on a 7-point scale of 1 (never true) to 7 (always true) designed to measure the relationship a person has with his or her own thoughts and beliefs
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Hospital Anxiety and Depression Scale (HADS; Zigmond, & Snaith 1983)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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A self-report rating scale of 14 items, designed to measure anxiety (HADS-A) and depression (HADS-D), with each subscale consisting of 7 items.
It consists of two sub-scales yielding a separate score for anxiety and depression.
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Present Moment Awareness Subscale of the Philadelphia Mindfulness Scale (Cardaciotto, Herbert, Forman, Moitra & Farrow, 2008)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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10-item self-report questionnaire that measures a key constituent of mindfulness
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Self-Compassion Scale-Short Form (Raes, pommier, Neff, & Van Gutcht, 2011)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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12-item measure that examines the relation of self-compassion to positive psychological health and the five-factor model of personality.
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Valuing Questionnaire (Smout, Burns & Christie, 2014)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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10-item measure that assesses the degree of personal values enactment "during the past week."
Items are rated on a 7-point scale ranging from 0 (not at all true) to 6 (completely true).
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Mental Health Continuum - Short Form (Keyes, 2005)
Time Frame: Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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14-item measure of positive mental health consisting of three sub-scales: Emotional well-being, psychological well-being, and social well-being.
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Baseline; 1-month post-baseline (post-intervention); 3-months post-baseline (follow-up)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Louise McHugh, PhD, University College Dublin
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HS19-13Murthy-McHugh
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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