Exploring the Suitability of Movement and Sound in Couple Therapy: A Proof-of-Concept Trial

Sponsor
University Medicine Greifswald (Other)
Overall Status
Completed
CT.gov ID
NCT04830553
Collaborator
Humboldt-Universität zu Berlin (Other)
30
1
2
12.2
2.5

Study Details

Study Description

Brief Summary

The present phase-IIA waiting-list controlled proof-of-concept trial aims to explore the adequacy of immediate sound feedback for physical distance and touch between individuals as a potential means to complement existing methods in couple therapy. The results obtained will determine the design of a subsequent phase-IIB randomized controlled trial.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Music-based couple therapy.
N/A

Detailed Description

According to early 20th century psychoanalysis, the "unsaid" becomes apparent in the relationship between patient and therapist, as well as in metaphors and symbols revealed through unintended utterances, imaginative techniques, and dreams. To convey emotions and thoughts, this method relies on the use of spoken language. Likewise, spoken language remains central to the practice of psychotherapy in subsequent decades, as clinicians and researchers sought to translate and transform major claims of psychoanalysis into newer paradigms, the most prominent of them being cognitive-behavioral, client-centered and family-systems psychotherapy. Inspired by somatic psychology and neuroscience evidence, more recent approaches focus on body and movement to target the "unsaid" beyond spoken language. Funded by the German Federal Ministry of Education and Research, the "Sentire" project attempts to provide immediate sound feedback for physical distance and touch between individuals (www.sentire.me). The present phase-IIA waiting-list controlled proof-of-concept trial aims to explore the adequacy of "Sentire" as a potential means to complement existing methods in couple therapy. The results obtained will determine the design of a subsequent phase-IIB randomized controlled trial.

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Exploring the Suitability of Movement and Sound in Couple Therapy: A Proof-of-Concept Trial
Actual Study Start Date :
Mar 26, 2021
Actual Primary Completion Date :
Apr 1, 2022
Actual Study Completion Date :
Apr 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Music-based couple therapy.

Each couple will receive five treatment sessions, including established methods from client-centered and family-systems psychotherapy as well as "Sentire," a technological approach providing immediate sound feedback for physical distance and touch. Duration of the treatment phase: five weeks.

Behavioral: Music-based couple therapy.
Each couple will receive five treatment sessions, including established methods from client-centered and family-systems psychotherapy as well as "Sentire," a technological approach providing immediate sound feedback for physical distance and touch. Duration of the treatment phase: five weeks.

No Intervention: Waiting list.

Each couple will go through an initial waiting period before the treatment phase. Duration of the waiting period: five weeks.

Outcome Measures

Primary Outcome Measures

  1. Change in Couples Satisfaction Index, CSI-32. [Change on the CSI-32, as determined by scores on this outcome measure at the beginning and immediately at the end of the five-week treatment phase or five-week waiting-list period.]

    This self-report questionnaire was conceived to quantify various aspects of a person's satisfaction in a couple relationship on a Likert scale ranging from 0 (very low satisfaction) to 6 (very high satisfaction).

Secondary Outcome Measures

  1. Change in Beck's Depression Inventory, BDI-II. [Change on the BDI-II, as determined by scores on this outcome measure at the beginning and immediately at the end of the five-week treatment phase or five-week waiting-list period.]

    This self-report measure of depression severity is known for its good psychometric properties, including construct validity and test-retest reliability.

  2. Change in ICD-10 Symptom Rating, ISR. [Change on the ISR, as determined by scores on this outcome measure at the beginning and immediately at the end of the five-week treatment phase or five-week waiting-list period.]

    This self-report measure based on the ICD-10 criteria of mental disorders serves as a screening instrument for psychological syndromes.

Other Outcome Measures

  1. Childhood Trauma Questionnaire, CTQ. [Beginning of the treatment phase. (Note: This outcome measure is only assessed once prior to the treatment phase.)]

    This self-report measure serves as a covariate to determine the relationship between childhood trauma and present issues in a couple relationship.

  2. Positive and Negative Affect Schedule, PANAS. [Change from beginning to end of each couple therapy session (i.e., outcome measure applied before and within 10 minutes after each meeting).]

    This self-report measure serves as an indicator of change in emotional arousal within each couple therapy session.

  3. Standortbestimmung. [Change from beginning to end of each couple therapy session (i.e., outcome measure applied before and within 10 minutes after each meeting).]

    This self-report measure serves as an indicator of subjective benefit from the treatment experienced within each couple therapy session.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • In couple relationship for at least six months;

  • Living in shared household or close daily contact.

Exclusion Criteria:
  • Currently acute episode of any mental disorder.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Humboldt-Universität zu Berlin Berlin Germany 10117

Sponsors and Collaborators

  • University Medicine Greifswald
  • Humboldt-Universität zu Berlin

Investigators

  • Principal Investigator: Benjamin Stahl, PhD, University Medicine of Greifswald

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
University Medicine Greifswald
ClinicalTrials.gov Identifier:
NCT04830553
Other Study ID Numbers:
  • SONIFY
First Posted:
Apr 5, 2021
Last Update Posted:
Apr 20, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 20, 2022