Evaluation of Three Tests to Assess Social Cognition in Huntington Disease
The Social-HD Study: A Cross-Sectional Observational Study of Social Cognition in Early Huntington Disease
1 other identifier
observational
40
1 country
1
Brief Summary
The goal of this observational study is to learn about the usefulness of a test of social functioning in persons with Huntington disease. Huntington disease affects motor function, psychological well-being and cognitive functions ("thinking abilities" such as paying attention, remembering and solving problems). It is also believed to affect important social functions, including the ability to understand others' intentions and emotions (social cognition). The test of interest in this study is called The Double Movie for the Assessment of Social Cognition-Multiple Choice (DMASC-MC) and will be compared to two other similar and well-known tests. The main question which the study aims to answer is: • Is DMASC-MC a useful tool for detecting problems with social functioning in adult persons with early Huntington disease? In the study, participants will meet with a medical doctor and a psychologist for assessment of different symptoms related to Huntington disease, including social functioning. Better methods for identifying problems with social functioning could help persons with Huntington disease and their families in mainly two ways. Firstly, it could increase their understanding of how the disease has affected them. Secondly, a better understanding of these problems could lead to better recommendations and interventions from medical teams, which would also benefit persons with Huntington disease and families.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Dec 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 17, 2025
CompletedFirst Posted
Study publicly available on registry
November 28, 2025
CompletedStudy Start
First participant enrolled
December 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2027
March 11, 2026
March 1, 2026
1.8 years
November 17, 2025
March 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Significant difference in mean value of "Double Movie for the Assessment of Social Cognition-Multiple Choice" (DMASC-MC) total score between HD and controls
To investigate if persons with HD have a significantly lower score than a control group in the test "Double Movie for the Assessment of Social Cognition-Multiple Choice" (DMASC-MC)". DMASC-MC: Minimum value 0, maximum value 44, higher scores mean a better outcome.
Baseline
Secondary Outcomes (10)
Significant difference in mean value of Reading the Mind in the Eyes Test (RMET) total score between HD and controls
Baseline
Significant difference in mean value of Emotional Hexagon Test (EHT) total score between HD and controls
Baseline
Significant correlation between social cognitive test scores and Montreal Cognitive Assessment (MOCA) scores
Baseline
Significant correlation between social cognitive test scores and total functional capacity (TFC) scores
Baseline
Significant correlation between social cognitive test scores and CAG-Age-Product (CAP) scores
Baseline
- +5 more secondary outcomes
Study Arms (2)
Huntington disease
Participants with early Huntington disease
Controls
Participants with no heritage of HD or negative pre-symptomatic HD gene test
Eligibility Criteria
Recruitment of participants will be made at the HD clinic in Lund, Sweden and through ethical review board-approved advertisment material posted at social media platforms and websites hosted by the Huntingtoncenter at Lund and the Swedish patient organization Riksförbundet för Huntingtons sjukdom (RHS) as well as YTAN.
You may qualify if:
- Clinical diagnosis of HD
- CAG repeat: 40 and more
- \. No heritage of HD or negative pre-symptomatic HD gene test
You may not qualify if:
- Participants in both groups are excluded from the study if any of the following criteria apply:
- Dementia or MOCA\<19, The Mini Mental State Examination (MMSE) \<19
- Other neurological disorders
- Ongoing psychosis
- Ongoing alcohol/drug addiction
- Other native language than Swedish
- Severe problems with vision and hearing
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Region Skanelead
Study Sites (1)
Skane University Hospital, Region Skane
Lund, 22184, Sweden
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Asa Petersen, MD PhD
Department of Psychiatry, Skåne University Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 17, 2025
First Posted
November 28, 2025
Study Start
December 1, 2025
Primary Completion (Estimated)
September 1, 2027
Study Completion (Estimated)
September 1, 2027
Last Updated
March 11, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share