NCT07253038

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
16mo left

Started Dec 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress25%
Dec 2025Sep 2027

First Submitted

Initial submission to the registry

November 17, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

November 28, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

December 1, 2025

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

March 11, 2026

Status Verified

March 1, 2026

Enrollment Period

1.8 years

First QC Date

November 17, 2025

Last Update Submit

March 10, 2026

Conditions

Keywords

social cognitionapathycognitiondepressiontotal functional capacitytotal motor score

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

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Skane University Hospital, Region Skane

Lund, 22184, Sweden

RECRUITING

Related Links

MeSH Terms

Conditions

Huntington DiseaseLethargyDepression

Condition Hierarchy (Ancestors)

Basal Ganglia DiseasesBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesDementiaChoreaDyskinesiasMovement DisordersHeredodegenerative Disorders, Nervous SystemNeurodegenerative DiseasesGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesCognition DisordersNeurocognitive DisordersMental DisordersNeurobehavioral ManifestationsNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsBehavioral SymptomsBehavior

Study Officials

  • Asa Petersen, MD PhD

    Department of Psychiatry, Skåne University Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Asa Petersen, MD, PhD

CONTACT

Isak Halling, MSc

CONTACT

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

Locations