The Effectiveness of Couple Therapy and Relationship Support (ECoT)
19 mai 2026 mis à jour par: Petra Nyman-Salonen, University of Helsinki
The Effectiveness of Couple Therapy and Relationship Support: a Randomized Controlled Trial
This randomized and controlled study investigates the effectiveness of relationship counselling and couple therapy in improving couples' relationship satisfaction and overall well-being. It compares four intervention groups both with each other and with a waitlist control group. The groups are:
- HUS Self-Help (Mielenterveystalo.fi): Participants independently complete online self-help tasks based on couple therapy, developed by Helsinki University Hospital (HUS) Psychiatry and Väestöliitto.
- Peloton Parisuhde (eng. Fearless Relationship) Online Course: Based on Emotionally Focused Couple Therapy (EFCT), this course by EFCT trainers Eklund-Mikola & Pinomaa uses online lectures and exercises to help couples identify negative interaction patterns and strengthen their emotional connection.
- Short Manualized Emotionally Focused Couple Intervention: Five face-to-face sessions with a couple therapist.
- Face-to-Face Couple Therapy (Treatment As Usual): 1 to 10 sessions, with the therapeutic approach varying depending on the therapist's training.
The study is conducted at the Relationship Counselling Unit of the City of Helsinki's Social Services in Finland, which provides counselling and family guidance under Section 26 of the Social Welfare Act to couples with children living in Helsinki. A total of 200 couples from the unit's treatment queue will be invited to participate and randomly assigned to one of the interventions or the control group, with 40 couples in each group.
Participants will complete questionnaires at the beginning and end of the service, and at a 4-month follow-up. The questionnaires measure relationship satisfaction and well-being, among other things. The study also examines how individual, couple-level, and treatment-related background factors influence and mediate the effectiveness of the interventions.
In addition to the questionnaires, registry data, therapist assessments, and ongoing treatment feedback collected within the unit is utilized. The results will provide new scientific insights into the effectiveness of short interventions and their suitable target groups and can be used to develop relationship counselling work both within the unit and nationally.
Aperçu de l'étude
Statut
Inscription sur invitation
Les conditions
Type d'étude
Interventionnel
Inscription (Estimé)
400
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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Helsinki, Finlande
- Relationship Counselling
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Oui
La description
Inclusion Criteria:
- Parents (couple) and blended families, and at least one of the parents is resident of Helsinki
- Couples expecting their first child. The couple is experiencing one or more of the following (1) severe relationship conflict, (2) a serious threat of separation, (3) significant challenges in forming a family or navigating a blended family relationship.
- couples eligible for treatment at the couple counselling faculty of Helsinki
Exclusion Criteria:
- Inadequate Finnish written language skills (the questionnaires are only available in Finnish)
- if both spouses do not complete the baseline questionnaires within the given deadline.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Soins de soutien
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
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Expérimental: HUS Self-help for Couples
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Self-Help Program for Couples (Mielenterveystalo.fi)
developed by HUS, this online self-help program provides couples with psychoeducational content and practical exercises designed to enhance relationship well-being.
Partners can complete the tasks together or individually.
The materials aim to strengthen emotional connection and improve communication.
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Expérimental: Peloton Parisuhde (eng Fearless Relationship) Online Course
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Based on Emotionally Focused Couple Therapy, this course by Eira Eklund-Mikola and Hanna Pinomaa uses online lectures and exercises to help couples identify negative interaction patterns and strengthen their emotional connection.
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Expérimental: Manualized Short-Term EFT-Based Couple Intervention
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Manualized Short-Term EFT-Based Couple Intervention is a structured program consisting of five face-to-face sessions with a trained couple therapist.
Based on Emotionally Focused Therapy (EFT), the intervention helps partners explore emotional patterns, improve communication, and strengthen their bond through guided therapeutic exercises.
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Expérimental: Standard Face-to-Face Couple Therapy (Treatment as Usual)
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This intervention consists of 1 to 10 in-person sessions with a couple therapist.
The therapeutic approach varies depending on the therapist's professional background and training.
It reflects typical clinical practice and is not standardized, allowing for flexibility in addressing the couple's specific needs.
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Aucune intervention: Waitlist (control group)
Participants in this group do not receive any intervention during the initial two-month study period.
After the waiting period, they are offered Treatment as Usual.
This group serves as a comparison to assess the effectiveness of the active treatments.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Relationship Satisfaction (Dyadic Adjustment Scale)
Délai: Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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The Dyadic Adjustment Scale (DAS) is a self-report questionnaire assessing relationship satisfaction and adjustment between romantic partners.
The scale measures consensus, satisfaction, cohesion, and affectional expression.
Total scores range from 0 to 151, with higher scores indicating better relationship adjustment and satisfaction.
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Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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Depression severity (Patient Health Questionnaire-9)
Délai: Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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The Patient Health Questionnaire-9 (PHQ-9) is a validated self-report measure assessing the severity of depressive symptoms over the past two weeks.
Total scores range from 0 to 27, with higher scores indicating more severe depressive symptoms.
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Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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Anxiety Severity (Generalized Anxiety Disorder-7)
Délai: Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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The Generalized Anxiety Disorder-7 (GAD-7) is a validated self-report measure assessing the severity of generalized anxiety symptoms over the past two weeks.
Total scores range from 0 to 21, with higher scores indicating more severe anxiety symptoms.
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Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Adult Attachment (Experiences in Close Relationships - Revised
Délai: Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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The Experiences in Close Relationships - Revised (ECR-R) is a widely used self-report questionnaire that assesses adult attachment styles in romantic relationships.
The instrument measures two dimensions: attachment anxiety and attachment avoidance, reflecting how individuals experience closeness, trust, and emotional connection with their partner.
Scores on each subscale typically range from 1 to 7, with higher scores indicating greater attachment anxiety or greater attachment avoidance.
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Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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Reflective Functioning (Reflective Functioning Questionnaire)
Délai: Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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The Reflective Functioning Questionnaire - RFQ-8 is a brief self-report measure developed by Fonagy and colleagues to assess reflective functioning, or mentalizing-the ability to understand one's own and others' thoughts, feelings, and intentions.
In couple research, it helps evaluate how well partners can interpret each other's behavior in emotionally meaningful ways, which is essential for healthy communication and emotional connection.
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Measured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup.
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Communication Patterns (Communication Patterns Questionnaire)
Délai: Masured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup
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Communication Patterns Questionnaire - Short Form (CPQ-SF) Developed by Christensen and Sullaway, the CPQ-SF is a self-report measure that assesses how couples communicate during conflict.
It focuses on typical interaction styles-such as constructive communication, avoidance, and demand-withdraw patterns-providing insight into how partners argue and resolve disagreements in their relationship.
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Masured at enrollment before randomization, after treatment (or waitlist condition) and at a 4 months followup
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Collaborateurs
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
11 novembre 2025
Achèvement primaire (Estimé)
31 décembre 2028
Achèvement de l'étude (Estimé)
30 juin 2029
Dates d'inscription aux études
Première soumission
12 mai 2026
Première soumission répondant aux critères de contrôle qualité
19 mai 2026
Première publication (Réel)
22 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
22 mai 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
19 mai 2026
Dernière vérification
1 mai 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- nro 20/2024
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Description du régime IPD
Individual participant data cannot be shared due to strict confidentiality and data protection regulations.
These data contain sensitive health-related information and personal identifiers, and sharing them could compromise participants' privacy.
All data are handled in accordance with ethical guidelines and legal standards to ensure the protection of participants' rights and well-being.
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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