- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05194683
The Effects of Relational Letter Writing
The Effects of Relational Letter Writing in Couples Wellbeing: A Mixed-Method Approach
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Adrian Montesano
- Phone Number: 0034934505225
- Email: amontesano@uoc.edu
Study Contact Backup
- Name: Kevser Cakmak
- Phone Number: 0034644387345
- Email: kcakmak@uoc.edu
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Investigators
- Principal Investigator: Adrian Montesano, Universitat Oberta de Catalunya
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- Study Protocol
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.