A Compassion-based Intervention for Internal and External Shame

November 30, 2021 updated by: Michael J. Telch, University of Texas at Austin
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.

Study Overview

Detailed Description

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.

Study Type

Interventional

Enrollment (Actual)

439

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Austin, Texas, United States, 78705
        • The University of Texas at Austin

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Self-compassion only
Describing a shameful experience using a self-compassionate prompt and receiving no verbal responses from confederates
Participants will be instructed to describe a shameful experience to two confederates using a self-compassionate prompt
Other Names:
  • Self-compassionate prompt
Following the participant's description of a shameful experience, two confederates will not be allowed to provide any verbal response
Other Names:
  • Neutral confederates
EXPERIMENTAL: Compassion from others only
Describing a shameful experience using a neutral prompt and receiving compassionate responses from confederates
Following the participant's description of a shameful experience, two confederates will respond with compassionate responses
Other Names:
  • Compassionate confederates
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
EXPERIMENTAL: Self-compassion plus compassion from others
Both describing a shameful experience using a self-compassionate prompt and receiving compassionate responses from confederates
Participants will be instructed to describe a shameful experience to two confederates using a self-compassionate prompt
Other Names:
  • Self-compassionate prompt
Following the participant's description of a shameful experience, two confederates will respond with compassionate responses
Other Names:
  • Compassionate confederates
ACTIVE_COMPARATOR: Sharing-only control
Describing a shameful experience using a neutral prompt and receiving no verbal responses from confederates
Following the participant's description of a shameful experience, two confederates will not be allowed to provide any verbal response
Other Names:
  • Neutral confederates
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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Internal shame
Time Frame: One-week post-intervention
Measured by scores on Internalized Shame Scale (range: 0-120, higher indicates more shame)
One-week post-intervention
Internal shame
Time Frame: 5 minutes post-intervention
Measured by scores on Internalized Shame Scale (range: 0-120, higher indicates more shame)
5 minutes post-intervention
External shame
Time Frame: One-week post-intervention
Measured by scores on Other As Shamer Scale (range: 0-72, higher indicates more shame)
One-week post-intervention
External shame
Time Frame: 5 minutes post-intervention
Measured by scores on Other As Shamer Scale (range: 0-72, higher indicates more shame)
5 minutes post-intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Shame activation
Time Frame: 5 minutes post-intervention
Real-time assessment of shame activation during shame memory recall tasks (range: 0-100)
5 minutes post-intervention
Shame activation
Time Frame: one-week follow-up
Real-time assessment of shame activation during shame memory recall tasks (range: 0-100)
one-week follow-up
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)
5 minutes post-intervention
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)
one-week follow-up
Electrodermal response to shame
Time Frame: 5 minutes post-intervention
Measured in microsiemens (μS) by Empatica E4 during shame memory recall tasks
5 minutes post-intervention
Electrodermal response to shame
Time Frame: one-week follow-up
Measured in microsiemens (μS) by Empatica E4 during shame memory recall tasks
one-week follow-up
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
5 minutes post-intervention
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
one-week follow-up
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
5 minutes post-intervention
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
one-week follow-up
Skin temperature reaction to shame
Time Frame: 5 minutes post-intervention
Temperature measured in degrees Celcius by Empatica E4 during shame memory recall tasks
5 minutes post-intervention
Skin temperature reaction to shame
Time Frame: one-week follow-up
Temperature measured in degrees Celcius by Empatica E4 during shame memory recall tasks
one-week follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Michael J Telch, PhD, Professor of Psychology

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

February 12, 2019

Primary Completion (ACTUAL)

November 18, 2021

Study Completion (ACTUAL)

November 18, 2021

Study Registration Dates

First Submitted

October 10, 2020

First Submitted That Met QC Criteria

October 18, 2020

First Posted (ACTUAL)

October 23, 2020

Study Record Updates

Last Update Posted (ACTUAL)

December 1, 2021

Last Update Submitted That Met QC Criteria

November 30, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 2018-07-0058

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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