This is the classic website, which will be retired eventually. Please visit the modernized ClinicalTrials.gov instead.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Oxford Social Movement Activation Study (SOMA)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT05963581
Recruitment Status : Recruiting
First Posted : July 27, 2023
Last Update Posted : February 22, 2024
Sponsor:
Information provided by (Responsible Party):
University of Oxford

Brief Summary:

For adolescents and young people particularly, there is need for better and more readily available treatments for depression and low mood. Comparatively less work has been done to characterize and treat depression specifically in young people. Previous literature indicates that often the unaddressed or under-addressed mental health difficulties in youth perseverate into adulthood and contribute to a host of individual and communal difficulties throughout the lifespan. Specifically, if depression goes unaddressed in young adulthood, the likelihood of a chronic course and multiple relapses or recurrences is much higher.

In the present research, we seek to investigate the potential efficacy of a novel intervention for young people with low mood. Depression disrupts social functioning, and social connectedness is especially important during adolescence for healthy development. Within a growing body of literature, social dance has been linked to social and mental health benefits along the dimensions of those disrupted in depression. We hypothesize that social dance might preferentially and efficiently target the goals of addressing loneliness, closeness, and enjoyment in young people compared to other approaches to the treatment of low mood and depression in a way that could lead to mood improvements.

Specifically, we are interested in the impact of a social movement-based activity, salsa dancing, on young peoples' mood and social and emotional processing. Social and emotional processing (SEP) tasks, such as emotional facial recognition and memory for emotional words, have been demonstrated to correspond with early changes that can be predictive of mood changes and treatment efficacy downstream. Including SEP tasks in this research will help to elucidate the potential mechanisms underlying mood improvements, should social dance correspond to improved mood in participants.

The present research seeks to:

  1. Aim 1: Investigate the effect of a social dance intervention on low mood. This will be assessed by administering psychological questionnaires to participants before, during, and after the study course of social dance sessions. In particular, we hypothesize that participants will experience reductions in low mood (assessed via the PHQ-9) following the social movement intervention as compared to a waitlist control.
  2. Aim 2: Characterize any early social and emotional processing changes that correspond to social dance versus a waitlist control. This will be assessed via social and emotional processing task performance before, during, and following the social movement sessions. We anticipate that improvements in social and emotional functioning as demonstrated via one or several of these tasks will assist in elucidating the possible mechanisms responsible for mood improvement from social movement.
  3. Aim 3: Characterize any social interaction difference from pre to post intervention that correspond to the social dance versus waitlist condition. This will be assessed via a version of the trust game before and following the social movement sessions and waitlist control. We anticipate seeing more disrupted trust behavior prior to the intervention or control conditions and less disrupted trust behavior following salsa dancing classes, but not the waitlist control.

In this randomized controlled trial, participants in the experimental group will complete six to eight sessions of social movement (salsa dance) classes within an eight-week period, and complete psychological questionnaires and tasks before, during, and after these eight weeks. Their scores will be compared with those of a control group that will participate in an active waitlist condition.

If the present study suggests that social movement benefits young people with low mood, it could form the basis for investigating a potential new cost-effective, non-invasive, accessible intervention that could be made available to young people.


Condition or disease Intervention/treatment Phase
Depression Low Mood Depressive Disorder Mood Disorders Depressive Symptoms Behavioral: Salsa Dancing Not Applicable

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 92 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Participants will be randomly assigned to either the salsa dancing intervention (46 participants) or the passive waiting-list control group (46 participants). Randomization will be stratified by gender.
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: Investigating the Effects of Social Movement on Mood and Social and Emotional Functioning in Young People Experiencing Low Mood
Actual Study Start Date : July 17, 2023
Estimated Primary Completion Date : July 16, 2024
Estimated Study Completion Date : July 16, 2024

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Salsa Dancing
Participants will complete eight weeks of a salsa course in Oxford (of which they need to attend six classes to remain in the study), followed by a one-month follow-up time point.
Behavioral: Salsa Dancing
Participants will complete salsa dancing classes in central Oxford with instructor(s) from the Oxford University Salsa Society

No Intervention: Waitlist Control
Participants will wait twelve weeks, completing the questionnaires and tasks at the same study time points as participants in the experimental condition.They will then be offered the opportunity to complete the eight-week salsa course. Should they choose to participate in the salsa course, they will additionally be offered the opportunity to complete questionnaires at two additional time points.



Primary Outcome Measures :
  1. Change in depressive symptoms from baseline at week four, eight, and twelve [ Time Frame: Will be assessed at week 0, 4, 8, and 12 of the intervention ]
    Patient Health Questionnaire (PHQ-9) score. Higher scores indicate greater depressive symptoms.


Secondary Outcome Measures :
  1. Change in anxiety symptoms from baseline at week four, eight, and twelve [ Time Frame: Will be assessed at week 0, 4, 8, and 12 of the intervention ]
    Generalized Anxiety Disorder Scale (GAD-7) score. Higher scores indicate greater anxiety.

  2. Change in social anxiety symptoms from baseline at week four, eight, and twelve [ Time Frame: Will be assessed at week 0, 4, 8, and 12 of the intervention ]
    Social Anxiety Scale - Adolescent (SAS-A) score. Higher scores indicate greater social anxiety.

  3. Change in loneliness from baseline at week four, eight, and twelve [ Time Frame: Will be assessed at week 0, 4, 8, and 12 of the intervention ]
    UCLA Loneliness Scale (+ Loneliness Question) score. Higher scores indicate more loneliness.

  4. Change in daily mood questionnaire scores [ Time Frame: daily from baseline through week 12 of the intervention ]
    Scoring one Likert scale mood questionnaire ("How happy do you feel?"), range 1-10. Higher values represent more happiness.

  5. Change in social anhedonia from baseline at week four, eight, and twelve [ Time Frame: Will be assessed at week 0, 4, 8, and 12 of the intervention ]
    Anticipatory and Consummatory Interpersonal Pleasure Scale (ACIPS) score. Higher scores indicate lower social anhedonia.

  6. Change in recognition of positive and negative facial expressions from baseline at week 8 [ Time Frame: Will be assessed at week 0 and week 8 of the intervention ]
    Hit rate for detecting positive versus negative faces in a facial expression recognition task (FERT)

  7. Change in speed during recognition of positive and negative facial expressions [ Time Frame: Will be assessed at week 0 and week 8 of the intervention ]
    Reaction times for correctly recognised positive versus negative faces in facial expression recognition task (FERT)

  8. Change in emotional categorisation (ECAT) [ Time Frame: Will be assessed at week 0 and week 8 of the intervention ]
    Reaction times for correctly classifying positive versus negative personality characteristic words

  9. Change in recall in the emotional recall task (EREC) [ Time Frame: Will be assessed at week 0 and week 8 of the intervention ]
    Number of positive and negative words correctly (and incorrectly) recalled in the EREC task

  10. Change in memory in the emotional memory task (EMEM) [ Time Frame: Will be assessed at week 0 and week 8 of the intervention ]
    Number of positive and negative words correctly (and incorrectly) recalled as familiar and novel

  11. Change in trust behavior in the trust game (Trust Game) [ Time Frame: Will be assessed at week 0 and week 8 of the intervention ]
    Investment behavior and sensitivity to trustee's generosity when playing the role of the investor in a trust game



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 24 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Individuals aged 18 to 24 at time of eligibility screening;
  • Competency to give informed consent;
  • Individuals will *not* be excluded for a formal diagnosis of depression from a GP or other mental healthcare provider, nor for being presently or formerly on medication for depression; nor for presently or formerly attending talk therapies;
  • Individuals who do not meet the exclusion criteria specified below.

Exclusion Criteria:

  • Individuals with a PHQ-9 score of less than 5 (indicating no low mood) or greater than 19 (indicating a low mood that could be too severe for this research);
  • individuals who self-report a current or recent diagnosis of any psychotic disorder (e.g., bipolar, schizophrenia, schizoaffective disorder), substance use disorders, eating disorders, or personality disorders
  • individuals who self-report that they are unfit for light physical exertion;
  • individuals who regularly, or have regularly, attended partner dance classes or partner dance events within the last six months (as they would already be receiving the potential benefits we are investigating in this study);
  • and individuals for whom the Principal Investigator determines that the study is not suitable.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05963581


Contacts
Layout table for location contacts
Contact: Susannah Murphy, DPhil +44 (0)1865 618313 susannah.murphy@psych.ox.ac.uk
Contact: Catherine Harmer, DPhil catherine.harmer@psych.ox.ac.uk

Locations
Layout table for location information
United Kingdom
University of Oxford Recruiting
Oxford, United Kingdom, OX3 7JX
Contact: Susannah Murphy, DPhil         
Sponsors and Collaborators
University of Oxford
Publications:

Layout table for additonal information
Responsible Party: University of Oxford
ClinicalTrials.gov Identifier: NCT05963581    
Other Study ID Numbers: SOMA
First Posted: July 27, 2023    Key Record Dates
Last Update Posted: February 22, 2024
Last Verified: February 2024
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University of Oxford:
low mood, depression, social movement, dance, salsa dance
Additional relevant MeSH terms:
Layout table for MeSH terms
Depression
Depressive Disorder
Mood Disorders
Behavioral Symptoms
Mental Disorders