- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05519267
Mindfulness-based Social Work and Self-Care (MBSWSC) (MBSWSC)
A Randomised Trial of Mindfulness-based Social Work and Self-Care Among Social Workers
Social work is a stressful occupation with social workers at high risk of job-related stress and burnout. Mindfulness has been evidenced as a promising approach for improving: recovery from stress; behavioural responses to stress; and resilience.
The main aim of the study is to examine the efficacy of a bespoke, innovative, 6-session Mindfulness Intervention for social workers (MBSWSC) in reducing social worker stress, feelings of burnout, anxiety, low mood and improving well-being. The study will also compare outcomes from the MBSWSC with a briefer, condensed 3 session mindfulness programme (MBSC).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Social work is a stressful occupation with social workers at high risk of burnout. It is perhaps unsurprising then that research has focused on the impact of working conditions and work-related stress in this population. COVID has seemingly intensified pressures on frontline social workers, in turn adversely impacting their health and wellbeing.
Despite awareness of the impact of social work, job-related stress, and burnout, there remains a lack of evidence on the implementation and effectiveness of interventions to mitigate these aspects and improve outcomes for social workers. A novel, innovative approach, embedded in social work practice, is needed to support and improve social worker wellbeing. Mindfulness has emerged as a promising approach evidencing success in improving: recovery, cognitive, emotional and behavioural responses to stress. Mindfulness has also been highlighted as an approach by which resilience is strengthened. Mindfulness has been found to generate positive outcomes for those working in health and social care; promoting wellbeing, increasing levels of self-care and self-compassion, reducing stress, and combating burnout. Self-care (self-compassion) has been highlighted as an important promoter of positive health effects in social work.
Although possible benefits of mindfulness for social workers have been suggested, the evidence base to support this is scant, mainly due to a scarcity of mindfulness based intervention studies aimed at social workers. Traditionally there has been a lack of evidence on the effectiveness of briefer mindfulness programmes; with recognised programmes such as MBSR and MBCT requiring significant time commitments from participants which may not be suitable for practicing professionals. In light of this; there is a clear need for high quality RCTs to add to the evidence base in this area and to inform future provision.
With this in mind, this study looked to explore the efficacy of a bespoke, innovative, 6-session Mindfulness Intervention for social workers (MBSWSC). It also served to compare the outcomes from the MBSWSC programme with a modified, condensed 3 session mindfulness programme (MBSC).
More explicitly, this RCT aims to examine the:
- Efficacy of the MBSWSC programme at improving social worker stress, feelings of burnout, anxiety, low mood and well-being (primary outcomes).
- Effectiveness of MBSWSC in improving mindfulness, attention regulation, acceptance, self-compassion, non-attachment and aversion, worry and rumination (secondary outcomes).
- Differences between MBSWSC outcomes and outcomes on the MBSC
Methods: 93 participants providing consent to participate in the study were randomised to either the experimental (MBSWSC) or active control (MBSC) groups. 62 participants completed baseline measures; with post-intervention measures completed by 47 participants.
The primary outcome of the study is the efficacy of MBSWSC on social worker stress, feelings of burnout, anxiety, low mood and well-being and secondary outcomes. The secondary outcome of the study is the differences in outcomes for MBSWSC participants and participants on the modified, condensed (briefer) MBSC. Data will be collected pre-intervention, post-intervention and at 3 month follow-up.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Northern Ireland
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Belfast, Northern Ireland, United Kingdom, BT7 1NN
- Queen's University Belfast
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Frontline social work practitioner; Working in Northern Ireland; Aged 18 years and over
Exclusion Criteria:
- Social workers in strategic social work roles with no contact with clients
Study Plan
How is the study designed?
Design Details
- Primary Purpose: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: MBSWSC programme
The Experimental group will take part in the Mindfulness Based Social Work and Self Care (MBSWSC) programme (6 sessions).
MBSWSC will be facilitated by two accredited mindfulness practitioners, who are also qualified social workers.
Sessions will be supplemented by brief homework activities.
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MBSWSC is a unique mindfulness-based programme for social work and self-care which has been specifically developed for online delivery.
The MBSWSC programme is embedded within key cognitive and emotion regulation, and stress coping theory (Maddock et al. 2019a).
This programme combines mindfulness practices with psychoeducation with the aim of allowing participants to reduce any negative thinking about the past and future by learning skills that will allow them to focus on the present.
It will also focus on how to effectively apply these newly acquired mindfulness skills in social work practice.
The MBSWSC programme comprises 6x1.5 hour sessions, delivered weekly, over a 6 week period.
Homework, in the form of mindfulness practices, is given each week.
This will take approximately 20-30 minutes to complete, on 6 out of 7 days, each week.
Other Names:
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ACTIVE_COMPARATOR: MBSC Programme
The Active comparator group will take part in the Mindfulness and Self-compassion (MBSC) programme (3 sessions).
MBSC will be facilitated by two accredited mindfulness practitioners, who are also qualified social workers.
Sessions will be supplemented by brief homework activities.
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MBSC is a modified, condensed Mindfulness Based Intervention; with a key focus on self-compassion.
Key practices in this condensed programme were chosen for their relevance and utility to social workers.
The MBSC programme comprises 3x1 hour sessions delivered over a 6 week period, with one session every two weeks.
Homework, in the form of mindfulness practices, is given each week.
This will take approximately 20-30 minutes to complete, on 6 out of 7 days, each week.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Stress measured on the Perceived Stress Scale (PSS)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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The Perceived Stress Scale is a 10-item, reliable and valid, measure of perceived stress.
Scores on this scale can range from 0-40, with higher scores indicative of higher levels of stress
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Burnout measured on the Maslach Burnout Inventory (MBI)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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The Maslach Burnout Inventory is a 22-item, reliable and valid measure of work-related burnout.
The scale comprises 3 sub scales: burnout, depersonalisation, and personal achievement.
The burnout subscale was used in this study.
Scores on this sub scale can range from 0-42.
Scores of ≤17 on this subscale are indicative of low-level burnout; scores of 18-29 indicate moderate burnout; scores ≥30 indicate high level burnout.
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Anxiety measured on the Hospital Anxiety and Depression Scale (HADS-A)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Hospital Anxiety and Depression Scale is a 14-item, reliable and valid measure of anxiety and depression.
7 of the 14 items measure severity of anxiety (HADS-A).
Scores on this sub scale can range from 0-21.
HADS-A subscale scores of 0-7 are considered normal, whilst scores of 11 or more are classified as moderate to severe
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Wellbeing measured on the Warwick-Edinburgh Mental Well-being Scale (WEMWBS)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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The Warwick-Edinburgh Mental Well-being Scale is a 14 item, reliable and valid measure of mental wellbeing.
Scores on this scale can range from 14-70.
Lower Warwick-Edinburgh Mental Well-being Scale scores are indicative of poorer mental wellbeing
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Depression measured on the Hospital Anxiety and Depression Scale (HADS)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Hospital Anxiety and Depression Scale is a 14-item reliable and valid measure of anxiety and depression.
7 of the 14 items measure severity of depression (HADS-D).
Scores on this sub scale can range from 0-21.
HADS-D subscale scores of 0-7 are considered normal, whilst scores of 11 or more are classified as moderate to severe
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Mindfulness measured by on the Southampton Mindfulness Questionnaire (SMQ)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Southampton Mindfulness Questionnaire is a 16-item reliable and valid measure assessing elements of mindfulness in response to unpleasant thoughts and images.
Scores on this scale range from 0-96.
Higher scores on the Southampton Mindfulness Questionnaire are indicative of greater levels on mindfulness
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Self-compassion measured by on the Self-Compassion Scale (SCS)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Self-Compassion Scale is a 12-item reliable and valid measure of self-compassion.
Scores on this scale can range from 12-60.
Higher mean scores reflect higher levels of self-compassion
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Worry measured on the Penn State Worry Questionnaire (PSWQ)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Penn State Worry Questionnaire is a 16-item reliable and valid measure of measure of worry.
Scores on this scale can range from 16-80.
Higher scores on the Penn State Worry Questionnaire reflect higher levels of pervasive, intense, and uncontrollable worry
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Acceptance measured on the The Philadelphia Mindfulness - Acceptance Subscale (PHLMS-A)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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The Philadelphia Mindfulness - Acceptance Subscale is a 10-item reliable and valid measure of the mindfulness component of acceptance.
Total scores on this sub scale range from 10-50.
Lower scores on the Philadelphia Mindfulness - Acceptance subscale reflect higher levels of acceptance
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Non-attachment measured by the Southampton Mindfulness Questionnaire Non Attachment subscale (SMQ-LG)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Southampton Mindfulness Questionnaire Non Attachment subscale is a reliable and valid measure of Non-attachment.
Scores on this sub scale range from 0-24.
Higher scores on this sub scale are indicative of higher levels of non-attachment
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Aversion measured by the Southampton Mindfulness Questionnaire Aversion subscale (SMQ-Av)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Southampton Mindfulness Questionnaire Aversion subscale is a reliable and valid measure of Aversion.
Scores on this sub scale range from 0-24.
Higher scores on this sub scale are indicative of higher levels of aversion
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Rumination measured on the Rumination Reflection Questionnaire Rumination subscale (RRQ-R)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Rumination Reflection Questionnaire Rumination subscale is a 12-item measure of engagement in rumination.
Scores on this scale range from 12-60.
Higher scores on this scale are indicative of greater engagement in rumination
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Change in Attention Regulation (Decentering) measured on the Experiences Questionnaire - Decentring (EQ-D)
Time Frame: Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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xperiences Questionnaire - Decentring is an 11-item measure of attention regulation/decentering.
Scores on this scale range from 11-55.
Higher scores on the xperiences Questionnaire - Decentring reflect higher levels of attention regulation
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Pre-intervention (week 1); Post-intervention (week 8); 3-month follow-up (week 20)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Alan Maddock, PhD, University of Dublin, Trinity College
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- REF 204_2021
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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