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CompletedNCT07905833REACH-FORUpdated Oct 30, 2026

REACH Forgiveness Group Intervention Adapted for Refugees (REACH-FOR)

An interventional study of REACH-FOR in Psychological Well-being, Unforgiveness and Refugees, sponsored by Universidad Pontificia Comillas. Completed at 1 site in Spain. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by Universidad Pontificia Comillas · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 7 years 10 months after the study started (first participant enrolled Dec 2018, registered Oct 2026).
Updated Oct 30, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this study was to find out whether REACH-FOR, a group program that helps people work toward forgiving a past offense, is useful for refugees, including people who cannot read or write well. Many refugees have experienced violence and injustice, and holding on to resentment has been linked to poorer mental health. REACH-FOR adapts the REACH Forgiveness program (Recall, Empathize, Altruistic gift, Commit, Hold on) by replacing written exercises with oral, visual, and group activities and by using examples drawn from refugees' own stories. Eighteen adult refugees living in a temporary reception center in Portugal were randomly assigned to take part in REACH-FOR straight away or to join a waiting list and take part one week later. Participants answered questionnaires about unforgiveness, forgiveness, and well-being before and after the program and one month later.

Read the detailed description

REACH-FOR was developed through a community-based participatory research approach, drawing on a preliminary qualitative study with refugees and key informants, a literature review, and feedback from a community advisor and partner organization. It keeps the five-step REACH structure (Recall, Empathize, Altruistic gift, Commit, Hold on), the main objective of each session, and the overall dose of Worthington's (2006) group protocol: six 90-minute sessions over three consecutive days, delivered by the researcher with an interpreter for the participants' first language. Changes concerned accessibility and cultural fit rather than content.

In this randomized waiting-list controlled trial, 18 Somali refugees were randomized, stratified by sex, to immediate REACH-FOR (n = 9) or a one-week waiting list (n = 9). The waiting-list group received REACH-FOR after the post-waiting assessment. All participants completed a one-month follow-up. Questionnaires were available in English, Spanish, Portuguese, Arabic, and Somali and were administered offline with KoBo Toolbox.

The intervention had previously been piloted (June 2018) in a non-randomized study with two groups of refugees (n = 23) at the same center; the pilot is reported in the same article but is not part of this registration.

02

Conditions studied

  • Psychological Well-being
  • Unforgiveness
  • Refugees

Keywords

  • forgiveness
  • REACH Forgiveness
  • refugees
  • asylum seekers
  • group intervention
  • low literacy
  • community-based participatory research
  • well-being
03

In context

Psychological Well-Being

1,065 studies on the registry are indexed under Psychological Well-Being; 508 are open to participants now.

This study's enrollment of 18 is below the median of 109 across 904 interventional studies indexed under Psychological Well-Being.

Browse Psychological Well-Being studies →

Lead sponsor

Universidad Pontificia Comillas is the lead sponsor of 19 studies on the registry; 4 are open to participants now.

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

04

Who can participate

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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • (1) Legal age (18 years or older).
  • (2) Asylum seeker or refugee assisted by the temporary reception center where the study took place.

Exclusion criteria

Exclusion Criteria:

  • None
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
18 participants (actual)

Study arms

  • Experimental
    Immediate REACH-FOR

    Participants received the REACH-FOR group intervention immediately after the baseline assessment (n = 9).

    Behavioral: REACH-FOR

  • Other
    Waiting-list control

    Participants waited one week without intervention and were then offered and received REACH-FOR (n = 9).

    Behavioral: REACH-FOR

Interventions

  • BehavioralREACH-FOR

    Group-based forgiveness intervention adapted from Worthington's REACH Forgiveness model (Recall, Empathize, Altruistic gift, Commit, Hold on) for refugees, including people with low literacy. Six 90-minute sessions over three consecutive days (9 contact hours), delivered by the researcher with an interpreter for the participants' first language. Written exercises are replaced by oral, visual, and group activities, and examples are drawn from refugees' own accounts.

    Also known as: REACH Forgiveness adapted for refugees

06

What researchers measure

Primary outcomes

  1. Change in Transgression-Related Interpersonal Motivations Inventory-12 (TRIM-12) Score From Baseline to Post-intervention

    Revenge and avoidance motivations toward the offender of a specific offense identified by the participant (McCullough et al., 1998). 12 items rated 1-5; total score 12-60; higher scores indicate more unforgiveness.

    Time frame: Baseline and post-intervention or post-waiting period (approximately 1 week after baseline)

  2. Change in Decisional Forgiveness Scale (DFS) Score From Baseline to Post-intervention

    Intention to behave more forgivingly toward the specific offender (Worthington et al., 2007). 8 items rated 1-5; total score 8-40; higher scores indicate a firmer decision to forgive.

    Time frame: Baseline and post-intervention or post-waiting period (approximately 1 week after baseline)

  3. Change in Emotional Forgiveness Scale (EFS) Score From Baseline to Post-intervention

    Emotional forgiveness experienced toward the offender for the specific offense (Worthington et al., 2007). 8 items rated 1-5; total score 8-40; higher scores indicate more emotional forgiveness.

    Time frame: Baseline and post-intervention or post-waiting period (approximately 1 week after baseline)

  4. Change in Trait Forgivingness Scale (TFS) Score From Baseline to Post-intervention

    Disposition to forgive across time and situations (Berry et al., 2005). 10 items rated 1-5; total score 10-50; higher scores indicate greater forgivingness.

    Time frame: Baseline and post-intervention or post-waiting period (approximately 1 week after baseline)

  5. Change in Mental Health Continuum - Short Form (MHC-SF) Score From Baseline to Post-intervention

    Emotional, social, and psychological well-being over the past month (Keyes, 2005). 14 items rated 0-5; total score 0-70; higher scores indicate greater well-being.

    Time frame: Baseline and post-intervention or post-waiting period (approximately 1 week after baseline)

Secondary outcomes

  1. Change in Transgression-Related Interpersonal Motivations Inventory-12 (TRIM-12) Score From Baseline to 1-Month Follow-up

    Revenge and avoidance motivations toward the offender of the specific offense. Total score 12-60; higher scores indicate more unforgiveness.

    Time frame: Baseline and 1 month after completing the intervention

  2. Change in Decisional Forgiveness Scale (DFS) Score From Baseline to 1-Month Follow-up

    Intention to behave more forgivingly toward the specific offender. Total score 8-40; higher scores indicate a firmer decision to forgive.

    Time frame: Baseline and 1 month after completing the intervention

  3. Change in Emotional Forgiveness Scale (EFS) Score From Baseline to 1-Month Follow-up

    Emotional forgiveness toward the offender for the specific offense. Total score 8-40; higher scores indicate more emotional forgiveness.

    Time frame: Baseline and 1 month after completing the intervention

  4. Change in Trait Forgivingness Scale (TFS) Score From Baseline to 1-Month Follow-up

    Disposition to forgive across time and situations. Total score 10-50; higher scores indicate greater forgivingness.

    Time frame: Baseline and 1 month after completing the intervention

  5. Change in Mental Health Continuum - Short Form (MHC-SF) Score From Baseline to 1-Month Follow-up

    Emotional, social, and psychological well-being over the past month. Total score 0-70; higher scores indicate greater well-being.

    Time frame: Baseline and 1 month after completing the intervention

07

Study locations

1 site
  • Universidad Pontificia Comillas
    Madrid, Madrid 28015, Spain
08

References and documents

Individual participant data

Plan to share: No — De-identified data are available from the corresponding author upon reasonable request; public sharing is restricted to protect a vulnerable refugee population.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07905833
Lead sponsor
Universidad Pontificia Comillas
Responsible party
Angela Ordoñez Carabaño (Researcher, Universidad Pontificia Comillas) — Principal investigator
First posted
Oct 30, 2026
Start date
Dec 1, 2018
Primary completion
Jan 30, 2019
Completion
Jan 30, 2019
Last update
Oct 30, 2026

Study contacts

Ángela Ordóñez Carabaño, Ph.D.
principal investigator · Universidad Pontificia Comillas

Oversight

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

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