The Effects of Relational Letter Writing

May 17, 2022 updated by: Adrián Montesano, Universitat Oberta de Catalunya

The Effects of Relational Letter Writing in Couples Wellbeing: A Mixed-Method Approach

The main objective of this research is to explore the relational letter writing technique as an intervention for improving couples' relational well-being. This is a two-arm superiority randomized clinical trial. Sixty-eight couples will be monitored before, during, and after the intervention. To observe the effect of the relational letter, scores of couples who are in the intervention arm and control arm will be compared (between groups) as well as pre-post scores (within-group). The content of the letter writing will be qualitatively analyzed to explore the reconstruction of their ethical values. Results from both methods will be integrated in order to get an in-depth perspective of the newly developed intervention. It is expected to increase the array of available techniques to help couples improve their individual and relational well-being.

Study Overview

Status

Not yet recruiting

Detailed Description

Relational letter writing is a recently developed therapeutic tool within the framework of Narrative Therapy that consists of two interviews and a letter writing task, in which a meta-conversation between the relationship itself, the couple members, and the therapists is fostered. Although this specific therapeutic technique can be used within the therapy process, in this study, it is used as a brief stand-alone narrative intervention.

The main objective of this study is to investigate the efficacy of the innovative Relational letter writing technique as a brief intervention for couples with mild to moderate levels of conflict. Also, the investigators want to explore changes in couples' narratives after experiencing the letter-writing procedure, and whether this technique can lead to reconstructing the relationship ethics and to greater relational awareness and well-being. The following objectives will be observed in this study:

  • To explore the effects of Relational letter writing practice on couples' relational well-being
  • To assess changes in individual psychological well-being after the Relational letter writing intervention
  • To observe whether this technique can lead to reconstructing the relationship ethics and to greater relational awareness, and its relationship with the outcome
  • To observe whether there is a difference between successful and unsuccessful cases in terms of the content of the letters.

Study Type

Interventional

Enrollment (Anticipated)

68

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 Contact

Study Contact Backup

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

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Couples willing to participate in a relationship enhancing intervention
  • Couples should have been living together at least for 12 months

Exclusion Criteria:

  • Couples who are currently receiving any kind of psychotherapy
  • Participants presenting severe psychological disorders (Psychosis, substance abuse, major depression)
  • Presence of intimate partner violence or abuse
  • Participants presenting cognitive impairment or disability impeding them from writing or answering written information
  • High-conflicted couples as measured by the DAS (Scores below 70)

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 Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Arm
No intervention
Experimental: Letter Writing Arm
Relational letter writing intervention
The intervention consists of two interviews and a between-session writing task. In the first session, couples will be interviewed regarding their relationship story and preferences. Between the two sessions, each couple member will write a letter from their relationship point of view. In the second interview, the task is reviewed and paths for relationship improvement are outlined.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Dyadic Adjustment Scale (DAS)
Time Frame: The change of relational wellbeing will be evaluated for a week before the intervention (baseline), after the first session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention).
The change of relational well-being will be evaluated with DAS (Spanier 1976, 2001), which is developed to provide a global measure of relational satisfaction of each member, has 32 items with 5-point, 6-point, 7-point Likert scales as well as two dichotomous items. Scores range from 0 to 151, higher scores indicating more dyadic adjustment.
The change of relational wellbeing will be evaluated for a week before the intervention (baseline), after the first session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention).
Perceived Relational Change
Time Frame: Perceived relational change will be administrated at post intervention, 2 weeks and 3 months after the intervention
Single item measure, 7-point likert scale measuring perceived change in their relationship as a result fo the intervention
Perceived relational change will be administrated at post intervention, 2 weeks and 3 months after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical Outcomes in Routine Evaluation - Outcome Measure Spanish version (CORE-OM)
Time Frame: Individual wellbeing will be evaluated for a week before the intervention (baseline), after the first session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention).
Individual wellbeing will be evaluated with CORE-OM (trujillo et al., 2016). This is a brief measure of individual well-being with 34 items with 6-point Likert-type scale ranging from 0 (Not at all) to 4 (Most or all the time). It covers four subscales: well-being (four items), problems/symptoms (12 items), life functioning (12 items), and risk to self and others (six items).
Individual wellbeing will be evaluated for a week before the intervention (baseline), after the first session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention).
Change in Global Measure of Relational Satisfaction (GMRS)
Time Frame: The change of relationship satisfaction will be evaluated a week before the intervention (baseline), after the first and second session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention)
The change of relational satisfaction will be evaluated with GMRS (Byers 2005) which is a six-item self-report questionnaire that measures an individual's relationship satisfaction with his/her current partner. Questions are 7-point Likert scale ranging from 1 to 7, minimum and maximum scores are 6 and 42, respectively, and lower scores indicate lower satisfaction in the relationship.
The change of relationship satisfaction will be evaluated a week before the intervention (baseline), after the first and second session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention)
Change in Outcome Rating Scale (ORS)
Time Frame: Chance of session to session progress will be evaluated a week before the intervention (baseline), after the first and second session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention).
Change of Outcome Rating Scale (ORS; Duncan et al., 2005) is an ultra-brief self-report measure that is designed to evaluate session-to-session progress made in therapy in terms of four domains. Participants will respond to how they are doing individually (personal well-being), socially (work, school, friendships), interpersonally (family, close relationships), and overall (general sense of well-being). For each item, place a mark on a 10-cm line. The mark indicates a positive feeling if it is marked to the right and it indicates a negative feeling if it is marked to the left on the line for each of the domains. The highest score possible is 40.
Chance of session to session progress will be evaluated a week before the intervention (baseline), after the first and second session of the interview, and with follow-ups (right after the intervention, 2 weeks, and 3 months after the intervention).

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Adrian Montesano, Universitat Oberta de Catalunya

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 (Anticipated)

June 15, 2022

Primary Completion (Anticipated)

December 31, 2022

Study Completion (Anticipated)

May 31, 2023

Study Registration Dates

First Submitted

December 14, 2021

First Submitted That Met QC Criteria

January 3, 2022

First Posted (Actual)

January 18, 2022

Study Record Updates

Last Update Posted (Actual)

May 18, 2022

Last Update Submitted That Met QC Criteria

May 17, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 1005988

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

Participant data for all primary and secondary outcomes, after deidentification.

IPD Sharing Time Frame

Data will be available after six months of study completion

IPD Sharing Access Criteria

Researchers who provide a methodologically sound proposal whose proposed use of the data has been approved by an independent review committee

IPD Sharing Supporting Information Type

  • Study Protocol

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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