Feasibility of the Internet Attachment-Based Compassion Therapy (iABCT)

June 10, 2021 updated by: Daniel Campos Bacas, Universitat Jaume I

The Feasibility of the Internet Attachment-Based Compassion Therapy (iABCT) for General Population

The purpose of this study is to investigate the feasibility, acceptability and preliminary efficacy of the internet Attachment-based compassion Therapy (iABCT) to promote wellbeing and mental health for the general population.

A feasibility open trial and single-arm study will be conducted with three measurement points: at baseline (pre-intervention), immediately after the intervention (post-), and 3-month follow-up, where participants will be allocated to iABCT.

To the best of our knowledge, this is the first study to explore the feasibility and preliminary efficacy of Compassion-based Intervention (CBI) delivered over the internet in Spanish.

Study Overview

Detailed Description

Compassion refers to a multidimensional psychological construct that involves the feeling that arises in presence of another's suffering and implies the desire to help. There is a growing number of studies pointing out the benefits of Compassion-based Interventions (CBI) and their association with psychological health. CBI are focused on training compassion to others and/or towards oneself (self-compassion) employing formal and informal meditation practices. Recent scientific literature is emerging to prove the feasibility and efficacy of cultivating compassion over the Internet and, thus, delivering self-applied online CBI.

The aim of this study is to investigate the feasibility and acceptability of the internet Attachment-based compassion Therapy (iABCT) to promote wellbeing and mental health for the general population. A secondary aim is to explore the preliminary efficacy of iABCT at post-intervention and 3-month follow-up.

The principal hypothesis is that the iABCT will be feasible and well-accepted by participants in terms of expectations, satisfaction, usability, opinion, and cost-effectiveness. Moreover, it is expected that the iABCT will be effective to promote changes in self-reported measures of compassion, self-compassion, mindfulness, self-criticizing, attachment, wellbeing, and mental health. It is also hypothesized that gains will be maintained at 3-month follow-up.

A minimum of 35 participants is considered enough to cover the aims of this feasibility study and to provide precise and efficient estimations of parameters (i.e., means, standard deviations, effect size, and confidence intervals) for powering a larger randomized controlled trial (RCT).

Study Type

Interventional

Enrollment (Actual)

50

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

      • Zaragoza, Spain, 50015
        • Centro de Salud Arrabal

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

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Be 18 years old or over.
  • Have adequate knowledge to understand and read Spanish.
  • Have a computer with speakers and Internet access in a secure setting (home or private office).
  • Have an email account.
  • Ability to use a computer and to surf the Internet.

Exclusion Criteria:

  • Diagnosis of mental disorder according to the Diagnostic and Statistical Manual for Mental Health Disorders-Version 5 (DSM-5).
  • Abuse or dependence on alcohol or other substances.
  • Be receiving psychiatric or psychological treatment,
  • Be engaged in ongoing formal meditation training (e.g., mindfulness or compassion intervention).
  • Presence of heart disease, cardiorespiratory illness, or other severe medical condition.
  • History of epileptic crisis.
  • Unavailability to complete the online intervention because of operation or medical intervention.

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: OTHER
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: internet Attachment-Based Compassion Therapy (iABCT)

The intervention will consist of an internet version of Attachment-Based Compassion Therapy (iABCT).

The length of the intervention will depend on the pace of each participant that will be advised to carry out one module per week, taking days between sessions to complete homework assignments. It is estimated that the online intervention can be completed in eight weeks, with a maximum period of ten weeks. However, each participant will be free to advance at his/her own pace. Formal telephone support will be not systematically provided, but participants will contact for technical assistance (i.e., web accessibility problems or forgotten password) if necessary.

The internet version of Attachment-Based Compassion Therapy (iABCT) will be developed to be totally self-applied over the Internet through the website www.psicologiaytecnologia.com designed by Labpsitec (Laboratory of Psychology and Technology, Universitat Jaume I, and University of Valencia). The iABCT will consist of eight sequential modules: Module 0) Welcome module: approaching to the compassion; Module 1) Preparing ourselves for compassion. Kind attention; Module 2) Discovering our compassionate world; Module 3) Developing our compassionate world; Module 4) Understanding our relationship with compassion; Module 5) Working on ourselves; Module 6) Understanding the importance of forgiveness; Module 7) Consolidating the practice of compassion

The content will present through texts, audios, videos, pictures, vignettes, and interactive exercises. Downloadable PDF files will be available so that users can review them offline.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Pemberton Happiness Index (PHI) (Hervás & Vázquez, 201)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
PHI is a measure of well-being that contains 11 items (in a scale from 0 to 10 point) related to different domains of remembered wellbeing, and 10 items related to experienced well-being (i.e., 5 positive and 5 negative emotional events that might have happened the day before) (answering YES/NO). The sum of these items produces a combined well-being index ranging from 0 to 10. Higher values represent higher wellbeing.
Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Self-Compassion Scale (SCS-26) (Neff, 2003; García-Campayo et al., 2014)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
The Self-Compassion Scale (SCS-26) is a 26-item questionnaire designed to assess overall self-compassion (total score) and three self-compassion facets: self-kindness (SCS-SK), common humanity (SCS-CH) and mindfulness (SCS-M). The Spanish version of the SCS-26 has shown high internal consistency and high test-retest reliability. The items are rated on a five-point Likert scale with 1 indicating almost never and 5 indicating almost always. After reversing the negatively formulated items, higher scores indicate greater self-compassion.
Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in Compassion Scale (Pommier, 2000)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
The Compassion Scale assesses compassion for others in similar dimensions to self-compassion. Responses are given on a 5-point scale ranging from 1 (almost never) to 5 (almost always). Pommier's (2010) results suggest that this scale presents good internal consistency and adequate convergent validity. A Spanish adaptation of Pommier's scale was developed for Brito-Pons (2014). The English version was translated by the researcher and refined with a team of psychologists and mindfulness instructors following a committee approach (Graham et al. 2003); finally, it was back-translated by native English speakers. Higher scores indicate greater compassion.
Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in Forms of Self-Criticizing/Attacking and Self-Reassuring Scale-Short form (FSCRS-SF) (Sommers-Spijkerman et al., 2017)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention

The FSCRS-SF contains 14 items to assesses two forms of self-criticism: inadequate self and hated self, and the ability to self-reassure.

Participants respond to a selection of statements, asking about how one thinks and reacts in the face of failures or setbacks, on a 5-point Likert scale ranging from 0 (not like me at all) to 4 (extremely like me). Higher scores indicate a greater sense of inadequacy, self-hate, or self-reassurance. The FSCRS-SF subscale scores had adequate test-retest reliability and satisfactory convergent validity estimates with theoretically related constructs.

Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in Five Facets of Mindfulness Questionnaire (FFMQ-15)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention

The FFMQ-15 is a short version of the FFMQ-39. This version includes 15 items to assess dispositional mindfulness rated on a Likert scale ranging from 1 (never or very rarely true) to 5 (very often or always true).

Five facets of mindfulness are assessed: Observe, refers to the subject's capacity to pay attention to internal and external experiences such as sensations, thoughts, or emotions; Describe, measures the ability to describe events and personal responses in words; Acting with awareness, includes focusing on the activity being carried out, as opposed to behaving automatically; Non-judging of inner experience, refers to the ability to take a non-evaluative stance toward thoughts and feelings; and Non-reactivity to inner experience, allowing thoughts and feelings to come and go, without getting caught up in them or carried away by them. The five scales show good internal consistency. Higher scores represent higher compassion.

Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in Relationships Questionnaire (RQ) (Bartholomew y Horowitz, 1991; Alonso-Arbiol y S.Yárnoz-Yaben, 2000).
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
The RQ uses a 7-point Likert-scale that assesses and matches participants with one of four attachment styles: (i) secure, (ii) pre-occupied, (iii) dismissive and (iv) fearful. A mathematical calculation permits a categorical assessment of attachment style (i.e. secure or insecure) (Griffin & Bartholomew 1994), and qualitative self-descriptor criteria can be used for confirmatory purposes. Studies have demonstrated that the reliability of the self-descriptor criteria is high (Leak and Parsons 2001; Yarnoz-Yaben and Comino 2011). The RQ also offers the possibility of measuring two key dimensions underlying attachment in adults (Griffin and Bartholomew 1994a)-namely, anxiety, which relates more to the self, and avoidance, which relates more to others (Griffin and Bartholomew 1994b). The anxiety dimension is calculated using the sum of the four attachment style ratings. High scores in this dimension reflect high anxiety towards social relationships.
Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in General Health Questionnaire (GHQ-12) (Rocha et al., 2011)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention

GHQ-12 is one of the most widely used screening tests to assess mental health of a population, and is designed as a structured, brief and self-administered questionnaire.

Every one of its 12 items regarding recent symptoms, feelings or behaviors is answered on a four-category Likert scale. Categories 1 and 2 are given value 0, and categories 3 and 4 are given value 1. Values from 12 items are added together to get an overall score. A probable psychiatric case is considered when the score is equal to or greater than 3.

Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in Non-Attachment Scale (NAS-7) (Feliu et al., 2016; Sahdra et al. 2015)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention

The NAS-7 is scored on a 6-point scale ranging from 1 = disagree strongly to 6 = agree strongly and designed to measure nonattachment (e.g., I can let go of regrets and feelings of dissatisfaction about the past when pleasant experiences end, I am fine moving on to what comes next).

The NAS-7 is unifactorial and shows excellent internal consistency (α = .82).

Higher scores represent higher nonattachment values.

Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in International Positive and Negative Affect Schedule Short Form (I-PANAS-SF; Thompson, 2007)
Time Frame: Before the intervention, during the intervention, immediately after the intervention, and 3-month follow-up after the intervention

The I-PANAS-SF -a reduced version of the PANAS- is composed of 10 items with 5-item Positive Affect (PA) Negative Affect (NA) subscales.

In a series of validation studies (N = 1,789), the cross-sample stability, internal reliability, temporal stability, cross-cultural factorial invariance, and convergent and criterion-related validities of the I-PANAS-SF were examined and found to be psychometrically acceptable.

Higher scores of PA subscale represent higher positive affect. Higher scores of NA subscale represent higher negative affect.

Before the intervention, during the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in Purpose-In-Life Test (PIL-10) (García-Alandete, Rosa, y Sellés, 2013; García-Galante, 2014)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
The PIL test is a 10-item self-report attitudinal scale designed to measure the extent to which a respondent perceives a general sense of meaning and purpose in life or respectively suffers from an "existential vacuum". The Spanish validation has shown to be a reliable measure to assess the meaning of life. Higher scores represent a higher sense of meaning and purpose in life.
Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Changes in Compassion Practice Quality Questionnaire(12 ítems) (adapted from Del Re et al., 2015).
Time Frame: During the intervention, immediately after the intervention, and 3-month follow-up after the intervention
The Compassion Practice Quality Questionnaire has been developed for this study to assess difficulties related to the practice of compassion meditation. This self-reported questionnaire includes 10 items that participant scores on a scale ranging from 0 to 100 indicating the percentage of time that his/her experience reflects each statement. Higher scores represent higher difficulties related to the compassion meditation practice.
During the intervention, immediately after the intervention, and 3-month follow-up after the intervention

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Attrition rate
Time Frame: Immediately after the intervention, and 3-month follow-up after the intervention
Percentage of participants that drop-out the intervention after having access for first time. Higher scores represent higher drop-out rates.
Immediately after the intervention, and 3-month follow-up after the intervention
Expectations and satisfaction Questionnaire (Adapted from Borkovec y Nau, 1972)
Time Frame: Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention

These questionnaires were adapted from Borkovec and Nau (1972) to measure participant expectations before the intervention and their later satisfaction with it.

Each scale includes six items rated from 0 ("not at all") to 10 ("very much"). The questions addressed how logical the intervention seemed, to what extent the participant expected to be satisfied with it, whether the participant would recommend the intervention to others, whether it would be useful for psychological problems, the interventions' usefulness for the participants, and to what extent it could be aversive (reverse item). Higher scores represent higher expectations and satisfaction levels.

Before the intervention, immediately after the intervention, and 3-month follow-up after the intervention
Acceptability and Usability Questionnaire (Labpsitec, 2019)
Time Frame: immediately after the intervention, and 3-month follow-up after the intervention
This instrument was adapted from the System Usability Scale (SUS) in order to assess the usability of a service or product and the acceptance of technology by the people who use it. The SUS has been shown to be a valuable and robust tool for assessing the quality of a wide range of user interfaces, as it is easy to use and understand. This scale includes 10 statements rated on a five-point scale measuring agreement with the statement (0 = strongly disagree; 4 = strongly agree). The final score is obtained by adding the scores on each item and multiplying the result by 2.5. Scores range from 0 to 100, where higher scores indicate better usability.
immediately after the intervention, and 3-month follow-up after the intervention
Qualitative opinion interview
Time Frame: immediately after the intervention
Qualitative Interview has been specifically developed to assess participant opinions about the internet intervention. This interview included 14 questions: seven of them regarding usefulness of the intervention, components, modules, information provided, and multimedia elements (e.g., images, audios, videos, pdf) rated on a scale from 1 to 5 (1 = very little; 2 = little; 3 = something; 4 = a lot; and 5 = very much) and two dichotomous questions ("yes" or "no") regarding whether they would like having at their disposal the program for more time after the treatment has finished, as well as whether they would like to have longer access. Additionally, options to extend the participants' qualitative responses were available. Finally, two open questions are included to assess advers or unwanted effects and facilitators and barriers towards the intervention received.
immediately after the intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Daniel Campos, PhD, Universitat Jaume I. Instituto de Investigación Sanitaria Aragón (IIS Aragón).

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.

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 20, 2020

Primary Completion (ACTUAL)

October 1, 2020

Study Completion (ACTUAL)

May 1, 2021

Study Registration Dates

First Submitted

April 11, 2019

First Submitted That Met QC Criteria

April 15, 2019

First Posted (ACTUAL)

April 17, 2019

Study Record Updates

Last Update Posted (ACTUAL)

June 14, 2021

Last Update Submitted That Met QC Criteria

June 10, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • UJaumeICO_CD/005/2019

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The raw IPD will be made available by the authors, without undue reservation, to any qualified researcher. Dataset will be available through scientific repositories and via email request.

IPD Sharing Time Frame

When the study is finished and results published.

IPD Sharing Access Criteria

The raw IPD will be made available by the authors, without undue reservation, to any qualified researcher.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

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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