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Studies how therapist and patient synchrony relates to depression treatment

Studies personal patterns of synchrony in adults with major depressive disorder receiving supportive-expressive therapy.

Key facts

Who runs it
University of Haifa
Where
Haifa, IsraelSee the site
Trial code
Registry title
An Individual-specific Synchrony Signature
Status
Recruiting
People taking part
78 people, planned
Started
22 Nov 2025
Expected to end
30 Mar 2030
Type of study
Interventional, 2 groupsOne group gets no study treatment, for comparison.
Treatments tested
  • Supportive-expressive treatment
Record updated
24 November 2025

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18 to 65 who currently have major depressive disorder and speak Hebrew. Participants take part in a talking therapy called supportive-expressive treatment.

Age
18 to 65 years
Sex
All sexes can join.
Disease stage
Current major depressive disorder (DSM-5), with a score above 14 on the 17-item Hamilton rating scale for depression at two assessments one week apart.
Earlier treatment
Anyone taking psychiatric medication must have had a stable dose for at least three months before the study. They are asked to keep the dose stable during treatment. People currently in psychotherapy cannot join.

Main reasons for not taking part

  • Current risk of suicide or self-harm
  • Current substance abuse disorder
  • Current or past schizophrenia, psychosis, bipolar disorder, or severe eating disorder needing medical monitoring
  • History of organic mental disease
  • Currently in psychotherapy

The registry criteria, word for word

Show all 10 criteriaShow less

Who can take part

  • Current major depressive disorder based on the Diagnostic and Statistical Manual of Mental Disorders-5, and scores above 14 on the 17-item Hamilton rating scale for depression at two consecutive assessments, one week apart
  • For participants using psychiatric medication, the dosage must be stable for at least three months before the beginning of the study, and they will be asked to maintain stable dosage during the treatment
  • Age between 18 and 65 years
  • Hebrew language proficiency
  • Provision of written informed consent

Who cannot take part

  • Current substance abuse disorders
  • Current or past schizophrenia or psychosis, bipolar disorder, or severe eating disorder requiring medical monitoring
  • History of organic mental disease
  • Current risk of suicide or self-harm
  • Currently in psychotherapy

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Where in Israel

  • University of HaifaHaifa, IsraelContact: Sigal Zilcha Mano, ProfessorTaking people

About the trial

What the trial wants to find out

This study aims to establish synchrony as an individual-specific mechanism of therapeutic change and offers novel insights into the mechanisms of curative interpersonal processes. The study identifies individual-specific trait-like synchrony signature and investigates the associations between synchrony signature, the individual's trait-like characteristics, and mental health, among participants diagnosed with Major Depressive Disorder. The study further investigates how deterministic the trait-like synchrony signature is by identifying for whom, how, and when changes are anticipated. Additionally, it examines whether synchrony signature transfers to relationships with the therapist, whether and how it changes throughout treatment, and whether such potential changes are associated with improvements in mental health. Synchrony is recognized as a key driver of collaborative, affiliative, and curative relationships. While its potential role in improving mental health through interpersonal relationships has sparked growing interest, particularly in psychotherapy, the field is at a crossroads, with mixed findings challenging the widespread theoretical assumption that "more synchrony is better." This study introduces a personalized framework that emphasizes individual-specific synchrony signatures, shifting from generalized assumptions to tailored understanding and interventions. The study explores how synchrony can transform relationships into curative ones by leveraging individual-tailored changes in synchrony signatures in psychotherapy. The potential impact is vast. Tailoring synchrony to individual-specific signatures represents a paradigm shift from a one-size-fits-all approach to personalized interventions. This personalized framework could revolutionize mental health care by facilitating the development of targeted strategies that enhance treatment outcomes.

The 2 groups in the trial

  • Supportive-expressive psychotherapyTreatment being tested

    Participants will receive supportive-expressive therapy for depressive disorder for 16 weeks.

    Treatment: Supportive-expressive treatment

  • Waiting listNo study treatment, for comparison

    Participants will wait for treatment for 16 weeks. After the waiting the participants will receive in a supportive-expressive treatment for depressive disorder for 16 weeks.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
An Individual-specific Understanding of How Synchrony Becomes Curative
Plain-language title
Studies how therapist and patient synchrony relates to depression treatmentGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Fit questions
Built from NCT06749392, who can take part
Record updated
24 November 2025