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Completed

NCT Number: NCT04600557

A Compassion-based Intervention for Internal and External Shame

This is a four-arm randomized pilot study aimed at reducing internal and/or external shame using self-compassion and/or compassion from others. The study is designed to test the theory that trait shame is comprised of both internal and external shame and to test compassion for others as an intervention for external shame.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University of Texas at Austin

Austin, Texas, 78705, United States

About this study

Shame is a common, painful emotion involving negative evaluations of the self. It has been theorized that trait shame involves both internal shame (i.e., evaluating oneself negatively) and external shame (i.e., perceiving that others evaluate the self negatively). Shame is experienced across a variety of psychiatric illnesses, yet it has been highly understudied.

Self-compassion has been used as an intervention for reducing shame in a variety of research studies, often in the context of a specific psychiatric disorder. However, self-compassion interventions, which aim to change the way one thinks and feels about oneself, may specifically target internal shame but not external shame. It is proposed that receiving compassion from others is an analogous and plausible intervention for external shame. In order to test the theory that trait shame is comprised of both internal and external shame and to test compassion for others as an intervention for external shame, a four-arm randomized pilot study aimed at reducing internal and/or external shame using self-compassion and/or compassion from others is proposed here.

Participants (N=180) scoring high on both internal and external shame on self-report measures will be assessed at baseline using both questionnaires and a shame-memory recall. Participants will be randomized to one of four conditions: a) describing a shameful experience using a self-compassionate prompt and receiving no verbal responses from confederates (self-compassion only), b) describing a shameful experience using a neutral prompt and receiving compassionate responses from confederates (compassion from others only), c) both describing a shameful experience using a self-compassionate prompt and receiving compassionate responses from confederates (self-compassion plus compassion from others), or d) describing a shameful experience using a neutral prompt and receiving no verbal responses from confederates (sharing-only control). Participants will complete questionnaires and shame-memory recalls again immediately following the sharing intervention and at a one-week post-intervention follow-up.

The two primary outcome measures will be state internal shame, as measured by the Internalized Shame Sclae, and state external shame, as measured by the Other As a Shamer scale. Both the Internalized Shame Scale and Other As a Shamer scale will be administered at baseline (immediately pre-treatment), immediately post-treatment, and a one-week post-intervention follow-up. Secondary outcome measures will include the Positive and Negative Affect Scale, and a real-time assessment of state shame.

It is expected that (a) participants assigned to describe a shameful experience using self-compassionate instructions will display larger reductions in internal shame relative to those assigned to describe a shameful experience using neutral instructions; (b) participants who receive compassionate responses from others after sharing a shameful experience will display larger reductions in external shame relative to those assigned to a listening-only control; and (c) participants assigned to describe a shameful experience using self-compassionate instructions combined with receiving compassionate responses from others will display larger reductions in both internal and external shame relative to participants who receive either component alone.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Elevated levels of internal and external shame
  • Can recall two shameful experiences

Exclusion criteria

  • Active suicidal ideation as measured by endorsement of 2 (I would like to kill myself) or 3 (I would kill myself if I had the chance) on BDI-II item 9
  • Endorses intent to harm or kill others

Treatment and study plan

Describing a shameful experience using a self-compassionate prompt

Behavioral

Participants will be instructed to describe a shameful experience to two confederates using a self-compassionate prompt

Other names: Self-compassionate prompt

Receiving compassionate responses from confederates

Behavioral

Following the participant's description of a shameful experience, two confederates will respond with compassionate responses

Other names: Compassionate confederates

Describing a shameful experience using a neutral prompt

Behavioral

Participants will be instructed to describe a shameful experience to two confederates using a neutral (i.e., not self-compassionate) prompt

Other names: Neutral prompt

Receiving no response from confederates

Behavioral

Following the participant's description of a shameful experience, two confederates will not be allowed to provide any verbal response

Other names: Neutral confederates

Primary outcomes

  1. Internal shame

    Time frame: One-week post-intervention

    Measured by scores on Internalized Shame Scale (range: 0-120, higher indicates more shame)

  2. Internal shame

    Time frame: 5 minutes post-intervention

    Measured by scores on Internalized Shame Scale (range: 0-120, higher indicates more shame)

  3. External shame

    Time frame: One-week post-intervention

    Measured by scores on Other As Shamer Scale (range: 0-72, higher indicates more shame)

  4. External shame

    Time frame: 5 minutes post-intervention

    Measured by scores on Other As Shamer Scale (range: 0-72, higher indicates more shame)

Secondary outcomes

  1. Shame activation

    Time frame: 5 minutes post-intervention

    Real-time assessment of shame activation during shame memory recall tasks (range: 0-100)

  2. Shame activation

    Time frame: one-week follow-up

    Real-time assessment of shame activation during shame memory recall tasks (range: 0-100)

  3. State shame

    Time frame: 5 minutes post-intervention

    Micro-assessment of state shame using Positive and Negative Affect Scale (range: 1-5, higher indicates more shame)

  4. State shame

    Time frame: one-week follow-up

    Micro-assessment of state shame using Positive and Negative Affect Scale (range: 1-5, higher indicates more shame)

  5. Electrodermal response to shame

    Time frame: 5 minutes post-intervention

    Measured in microsiemens (μS) by Empatica E4 during shame memory recall tasks

  6. Electrodermal response to shame

    Time frame: one-week follow-up

    Measured in microsiemens (μS) by Empatica E4 during shame memory recall tasks

  7. Blood volume pulse in reaction to shame

    Time frame: 5 minutes post-intervention

    Changes in blood volume measured by Empatica E4 during shame memory recall tasks

  8. Blood volume pulse in reaction to shame

    Time frame: one-week follow-up

    Changes in blood volume measured by Empatica E4 during shame memory recall tasks

  9. Motion in reaction to shame

    Time frame: 5 minutes post-intervention

    Measured by 3-axis accelerometer sensor in the range [-2g, 2g] using Empatica E4 during shame memory recall tasks

  10. Motion in reaction to shame

    Time frame: one-week follow-up

    Measured by 3-axis accelerometer sensor in the range [-2g, 2g] using Empatica E4 during shame memory recall tasks

  11. Skin temperature reaction to shame

    Time frame: 5 minutes post-intervention

    Temperature measured in degrees Celcius by Empatica E4 during shame memory recall tasks

  12. Skin temperature reaction to shame

    Time frame: one-week follow-up

    Temperature measured in degrees Celcius by Empatica E4 during shame memory recall tasks

Sponsors and collaborators

Lead sponsor

University of Texas at Austin

Other

Registry information

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Oct 23, 2020
Registry last updated
Dec 1, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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