CClinicalTrials.gg
CompletedNCT04984252Updated Oct 5, 2021

Testing a Brief and Low Intensity Self-compassion Intervention

An interventional study of Self-compassion comprising compassionate body scan-1, compassion body scan-2 and short noticing practice and Self-compassion comprising self-compassion break, loving kindness meditation, and breathing exercise. in Body Image Disturbance, Body Image and Shame, sponsored by University of Sheffield. Completed at 1 site in United Kingdom. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-10-05.

Sponsored by University of Sheffield · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
69
Allocation
Randomized
Ages
18 Years and older
Sex
Female
01

Study summary

The investigators' recent feasibility trial of a self-compassion and active control intervention showed that the self-compassion intervention was promising in reducing state body shame during a 40-minute intervention session. There were three time points where the reduction in the body shame level was significant, indicating three active components in the intervention that led to significant reduction in state body shame. It is unclear if a shorter self-compassion intervention based on only the active components would be as effective as the longer intervention at reducing state body shame. Such a short intervention then could be used as an in-session change method (15-20 mins) as part of a larger package, or as a homework exercise.

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Conditions studied

  • Body Image Disturbance
  • Body Image
  • Shame
03

In context

Lead sponsor

University of Sheffield is the lead sponsor of 74 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age ≥ 18 years
  • Self-identified women
  • Be able to use a computer and have an Internet connection

Exclusion criteria

Exclusion Criteria:

  • Insufficient knowledge of English
  • Learning disability or psychiatric illness requiring secondary care intervention
  • Male
  • Under 18 years old
  • No access to a tablet or computer with an internet connection
  • Body mass index below 18.5
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
69 participants (actual)

Study arms

  • Active comparator
    Only Active components

    15 minutes, once

    Behavioral: Self-compassion comprising compassionate body scan-1, compassion body scan-2 and short noticing practice

  • Sham comparator
    Inactive components

    15 minutes, once

    Behavioral: Self-compassion comprising self-compassion break, loving kindness meditation, and breathing exercise.

  • Placebo comparator
    Distraction group

    15 minutes, once

    Behavioral: Distraction group

Interventions

  • BehavioralSelf-compassion comprising compassionate body scan-1, compassion body scan-2 and short noticing practice

    This intervention includes 3 short meditations that are identified as the active component in the previous study (ID: NCT04665167)

  • BehavioralSelf-compassion comprising self-compassion break, loving kindness meditation, and breathing exercise.

    This intervention includes 3 short meditations that are identified as the inactive component in the previous study (ID: NCT04665167)

  • BehavioralDistraction group

    Participants will be asked to listen recording on irrelevant topic.

06

What researchers measure

Primary outcomes

  1. Change from baseline Subjective units of shame (SUS) at the end of the intervention

    Subjective units of shame (SUS), taken at four points during the intervention (scored 0 no shame to 100 full of shame)

    Time frame: through study completion, an average of 3 months

Secondary outcomes

  1. Body Image States Scale

    It will be used to assess transient feelings about the body and physical appearance. A 6-item scale measures current body-image experiences at a particular point in time or in a specific context. Possible scores range from 6 to 54, and higher scores indicate more positive body image (better outcome).

    Time frame: through study completion, an average of 3 months

  2. Shame subscale of the State Shame and Guilt Scale

    It will be used to test state shame. Possible scores are ranged from 5 to 25. Higher scores indicate worse state shame.

    Time frame: through study completion, an average of 3 months

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Study locations

1 site
  • Fidan Turk
    Sheffield, S1 2LT, United Kingdom
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 5, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04984252
Lead sponsor
University of Sheffield
Responsible party
Fidan Turk (Principal investigator, University of Sheffield) — Principal investigator
First posted
Jul 30, 2021
Start date
Aug 1, 2021
Primary completion
Sep 16, 2021
Completion
Sep 18, 2021
Last update
Oct 5, 2021

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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