Comparing three social cognition tests in adults with early Huntington disease
Official title: The Social-HD Study: A Cross-Sectional Observational Study of Social Cognition in Early Huntington Disease
Run by Region Skane · NCT07253038 · Data updated 2026-11-12
This project will test whether the DMASC-MC and two established social cognition tests can detect social thinking problems in adults with early Huntington disease.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Region Skane Academic / other |
| Locations | 1 site (Lund) |
| Status | Recruiting |
| Started | December 1, 2025 |
| Main results expected | September 1, 2027 |
| Study ends | September 1, 2027 |
| Registry record updated | March 11, 2026 |
| Trial ID | NCT07253038 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults with clinically diagnosed early-stage Huntington disease (CAG ≥40), fluent in Swedish, without dementia (MOCA/MMSE ≥19), and willing to attend assessments at the study site.
✕Probably not a fit
People with advanced cognitive impairment (MOCA/MMSE <19), active psychosis, substance addiction, other neurologic disorders, or who are not native Swedish speakers are unlikely to benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study will enroll 20 adults with early Huntington disease and 20 age- and sex-matched control participants to compare performance on three social cognition measures. Participants will complete the Double Movie for the Assessment of Social Cognition-Multiple Choice (DMASC-MC), the Reading the Mind in the Eyes Test, and the Emotion Hexagon Test, and will be assessed by a physician and a psychologist. Inclusion requires a clinical HD diagnosis with CAG ≥40 for the HD group and no family history or a negative pre-symptomatic gene test for controls, with exclusions for dementia (MOCA or MMSE <19), other neurological disorders, active psychosis, substance addiction, non-Swedish native language, or severe sensory deficits. The design is cross-sectional and powered for group differences between early HD and matched controls.
Why it matters
Potential benefit: If DMASC-MC proves sensitive, clinicians could better detect early social cognition problems and tailor support for people with early Huntington disease.
How similar studies have gone: Related social cognition tests have revealed deficits in Huntington disease and other neurodegenerative conditions, but the DMASC-MC is relatively new and has not been widely validated in HD.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Inclusion criteria for persons with HD 1. Clinical diagnosis of HD 2. CAG repeat: 40 and more Inclusion criteria for control group 1\. No heritage of HD or negative pre-symptomatic HD gene test Exclusion Criteria: Participants in both groups are excluded from the study if any of the following criteria apply: 1. Dementia or MOCA\<19, The Mini Mental State Examination (MMSE) \<19 2. Other neurological disorders 3. Ongoing psychosis 4. Ongoing alcohol/drug addiction 5. Other native language than Swedish 6. Severe problems with vision and hearing
Where it's running
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Skane University Hospital, Region Skane
Lund, Sweden Recruiting
Study contacts
- Principal investigator: Asa Petersen, MD PhD — Department of Psychiatry, Skåne University Hospital
- Study coordinator: Asa Petersen, MD, PhD
- Email: asa.petersen@med.lu.se
- Phone: +46462221686
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.