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CompassionNCT05589116

An Online Compassionate Imagery Intervention for Veterinarian Mental Health

A study testing Online Compassionate Imagery Intervention in people with Compassion and Perfectionism, run by University of Surrey at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This randomised control trial aims to determine the efficacy of a two-week, online compassionate imagery intervention on improving veterinarian mental wellbeing. Participants will be randomly allocated to receive the intervention immediately or after a 10-week study period. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Compassion, Perfectionism, Rumination
What is being tested?
Online Compassionate Imagery Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
162 participants
Where
1 siteUnited Kingdom
Study dates
29 Nov 2022to 14 Jul 2023
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

  • Any student, recent graduate or qualified veterinary surgeon will be eligible for participation in the study.

Who cannot join

  • Veterinarians who participated in Wakelin et al.'s (2022) feasibility trial.
  • Veterinarians who are currently receiving a compassion- or cognitive-based therapy.

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • University of Surrey

    Guildford, Middlesex, GU2 7XH

Other trials in United Kingdom

About this study

Official title: Investigating the Efficacy of a Two-week, Online Compassionate Imagery Intervention for Improving Mental Wellbeing in Veterinarians: A Randomised Controlled Trial

This randomised control trial aims to determine the efficacy of a two-week, online compassionate imagery intervention on improving veterinarian mental wellbeing. Participants will be randomly allocated to receive the intervention immediately or after a 10-week study period. Self-report questionnaires will be used at four time points to measure change on a range of psychological variables.

Read the detailed description

Background: Research suggests that veterinarians are high-achievers with self-critical, perfectionist tendencies (Holden, 2020). Perfectionism in veterinarians has been associated with stress, anxiety, negative affect and low resilience (Crane, Phillips \& Karin, 2015). However, McArthur et al. (2017) found that veterinarians with higher levels of self-compassion reported greater resilience. A feasibility study by Wakelin, Perman and Simonds (2022) found an online two-week compassion-focused imagery intervention to be acceptible and feasible for a veterinarian sample. Wakelin et al. (2022) also reported indications of preliminary effect as veterinarians illustrated a reduction in perfectionism, work-related rumination and self-criticism over the intervention period.

Aim: This study aims to extend Wakelin et al.'s (2022) research, to determine the efficacy of a two-week, online compassionate imagery intervention on improving veterinarian mental wellbeing.

Design: The study will use a mixed-methods, repeated measures, randomised controlled trial design.

The independent variables will be the intervention group (either treatment or wait list control) and the data collection time point. Six questionnaires will be used to collect quantitative data on the following dependent variables: perfectionism, work- related rumination, fear of compassion, resilience, self-compassion, self- criticism and self-reassurance.

Method: Participants will complete questionnaire measures at four time points: prior to randomisation (baseline), two weeks post-randomisation (post-intervention), six-weeks post-randomisation (one-month intervention follow-up) and ten-weeks after randomisation (two-month intervention follow up). Participants in the treatment group will be asked to watch a 10-15 minute compassionate imagery video every day for two weeks (14 in total). Participants in the control group will gain access to intervention materials upon study completion but their engagement in the videos will not be monitored.

Being tested
Online Compassionate Imagery Intervention
Medical subject headings
Rumination Syndrome

What participants receive

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

  • Online Compassionate Imagery InterventionOther

    The intervention comprises 14 pre-recorded, 10-15 minute videos. Participants will be asked to watch one video per day over a two-week period. The videos initially focus on providing psychoeducation about what self-compassion is, before delivering a series of guided Compassion Focused Therapy (CFT) informed exercises to cultivate self-compassion. The first week of the intervention will teach key compassion skills, with the second week focusing on skill consolidation.

Study groups in NCT05589116
Study groupRoleWhat they receive
Intervention groupExperimentalParticipants given immediate access to two-week, online compassionate imagery course.
Receives: Other: Online Compassionate Imagery Intervention
Wait-list control groupNo interventionParticipants will not access intervention during 10-week study period (access will be given to online compassionate imagery course after all outcome measures have been completed).

What is being measured

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

  1. Change in 'Functions of Self-Criticising/Attacking and Self-Reassuring Scale' (FSCRS; Gilbert, Clarke, Hempel, Miles & Irons, 2004).

    This 22-item scale will be used to measure self-criticism and self-reassurance. Participants are required to respond to statements on a 5-point Likert scale, ranging from 0 ('not at all like me') - 4 ('extremely like me'). The FSCRS has 3 subscales (Hated Self, Inadequate Self and Reassured Self) which are used to produce an overall self-criticism score (calculated by summing the Hated Self and Inadequate Self items) and a self-reassurance score (calculated by summing the Reassured Self items).

    Measured: 4 time points: baseline, immediate post-intervention, four weeks post-intervention and eight weeks post-intervention

Secondary outcomes (5)
  1. Change in 'Brief Resilience Scale' (BRS; Smith et al., 2008)

    This 6-item scale will be used to measure resilience. The scale uses a combination of positively and negatively worded statements, which participants must respond to on a Likert Scale ranging from 1 ('strongly disagree') to 5 ('strongly agree'). The scores are summed to produce a total score, with a higher total score reflecting a higher level of resilience.

    Measured: 4 time points: baseline, immediate post-intervention, four weeks post-intervention and eight weeks post-intervention

  2. Change in 'Compassionate Engagement and Action Scales' Self-Compassion scale (CEAS; Gilbert et al., 2017)

    The 13-item CEAS Self-Compassion scale will be used to measure self-compassion. It uses a series of statements, to which the participant must respond on a Likert Scale with responses ranging from 1 ('never') to 10 ('always'). The scale has two subscales, which are aligned with the two dimensions of Gilbert's (2017) model of compassion: 'Compassionate Engagement' and 'Compassionate Action'. A total score can be produced by summing the subscale scores, with a higher score reflecting a higher level of self-compassion.

    Measured: 4 time points: baseline, immediate post-intervention, four weeks post-intervention and eight weeks post-intervention

  3. Change in 'Work-related Rumination Questionnaire' (WRRQ; Cropley, Michalianou, Pravettoni & Millward, 2012)

    This 25-item scale will be used to measure a person's tendency to engage in ruminative thinking about work; participants will be asked to respond in relation to their university, placement, or clinic work. The WRRQ has three subscales (affective rumination, problem-solving pondering, and distraction detachment), and a mean total score is calculated, with higher scores indicating a higher level of rumination.

    Measured: 4 time points: baseline, immediate post-intervention, four weeks post-intervention and eight weeks post-intervention

  4. Change in 'Frost Multidimensional Perfectionism Scale - 24 Items' (FMPS-24; Khawaja & Armstrong, 2005).

    This 24-item scale will be used to measure perfectionism. The scale is scored out of 120, with a higher score indicating stronger perfectionistic tendencies.

    Measured: 4 time points: baseline, immediate post-intervention, four weeks post-intervention and eight weeks post-intervention

  5. Change in 'Fears of Compassion Scale' (FCS; Gilbert, McEwan, Matos & Rivis, 2011).

    This 38-item scale will be used to measure Fears of Compassion and it comprises three subscales: Fears of Compassion-Self, Fears of Compassion- For others, and Fears of Compassion- From others.

    Measured: 4 time points: baseline, immediate post-intervention, four weeks post-intervention and eight weeks post-intervention

Timeline

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

  1. First posted21 Oct 2022
  2. Study start29 Nov 2022
  3. Primary completion14 Jul 2023
  4. Study completion14 Jul 2023

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
Model description
Participants will be randomly allocated to either a treatment or wait-list control group. The study will use a repeated measures, randomised controlled trial design.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
162 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05589116
Sponsor's protocol ID
FHMS 21022 252 EGA
Status last verified
Sep 2023
First submitted
17 Oct 2022
Last updated
22 Sep 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Wakelin KE, Perman G, Simonds LM. Feasibility and efficacy of an online compassion-focused imagery intervention for veterinarian self-reassurance, self-criticism and perfectionism. Vet Rec. 2023 Jan;192(2):e2177. doi: 10.1002/vetr.2177. Epub 2022 Sep 10.

    PubMed 36087064
  • Holden CL. Characteristics of Veterinary Students: Perfectionism, Personality Factors, and Resilience. J Vet Med Educ. 2020 Jul;47(4):488-496. doi: 10.3138/jvme.0918-111r. Epub 2020 May 15.

    PubMed 32412364
  • Crane MF, Phillips JK, Karin E. Trait perfectionism strengthens the negative effects of moral stressors occurring in veterinary practice. Aust Vet J. 2015 Oct;93(10):354-60. doi: 10.1111/avj.12366.

    PubMed 26412116
  • McArthur M, Mansfield C, Matthew S, Zaki S, Brand C, Andrews J, Hazel S. Resilience in Veterinary Students and the Predictive Role of Mindfulness and Self-Compassion. J Vet Med Educ. 2017 Spring;44(1):106-115. doi: 10.3138/jvme.0116-027R1.

    PubMed 28206835

Questions about this trial

What is this clinical trial studying?

A study testing Online Compassionate Imagery Intervention in people with Compassion and Perfectionism, run by University of Surrey at 1 site in United Kingdom.

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 1 inclusion and 2 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: finished, as of the sponsor's last update on 22 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Change in 'Functions of Self-Criticising/Attacking and Self-Reassuring Scale' (FSCRS; Gilbert, Clarke, Hempel, Miles & Irons, 2004). (time frame: 4 time points: baseline, immediate post-intervention, four weeks post-intervention and eight weeks post-intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05589116, which also lists 4 linked publications.

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 22 Sep 2023.

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