CClinicalTrials.gg
CompletedNCT05250323BEHD-EMUpdated Feb 22, 2022

Energy Balance in Huntington's Disease. A Multidisciplinary Study Approach for a Complex Problem (BEHD-EM)

An observational study in Huntington Disease, sponsored by Hospital Universitario de Burgos. Completed at 1 site in Spain. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-02-22.

Sponsored by Hospital Universitario de Burgos · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
30
Ages
18 Years and older
Sex
All
01

Study summary

The study was conducted at the University Isabel I, Burgos in collaboration with the Hospital Universitario Burgos, Spain, through the creation of a multidisciplinary research team including graduates in physical activity and sports sciences, dietitians-nutritionists, neurologists and occupational therapists. To carry out this study: 1) the investigators used new technologies, specifically, small wearable or wearable devices available to the population. These devices measure their daily behaviour and estimate aspects such as energy expenditure, validated both in healthy participants and in participants with neurodegenerative diseases such as Parkinson's disease, but not in HD; 2) the investigators included a consecutive sample of patients with HD ; 3) the investigators performed the experimental study at the the laboratory for Exercise Physiology, Health and Quality of Life at the Isabel I University.

The hypothesis proposed by this study are the following: 1) Patients with HD who present an adequate energy balance caused by healthier lifestyles (active lifestyles and healthy eating) will present a better functional capacity, quality of life and therefore both less dependency; 2) HD patients with a balanced energy balance maintain adequate body composition (muscle, fat); 3) Adequate body composition is associated with better functional capacity in HD patients.

Read the detailed description

In the last decade, numerous studies have been published showing how epigenetic (environmental) factors can modify the clinical manifestations of diseases of genetic origin. Specifically, epidemiological studies have observed that physical exercise delays the onset and slows down the progression of neurodegenerative diseases (dementia, Parkinson's disease, HD), by producing, between the different mechanisms, greater plasticity of the different neuronal circuits. Another environmental factor such as nutrition has also been highlighted by numerous authors, highlighting the role of the Mediterranean diet in delaying the onset, especially in Parkinson's disease, as the phenolic components of olive oil produce an inhibition of the Pathological aggregation of modified alpha synuclein. On the contrary, it has been seen that an energy deficit at the cellular level accelerates the neurodegeneration process, shortening survival in different animal models.

To maintain an adequate energy balance, it is required that the energy expenditure produced by physical activity (GAF), plus the expenditure produced by the maintenance of the different organs: energy expenditure at rest (GAR) and thermogenesis, is similar to the input of energy produced by the oxidation of macronutrients from food intake. In HD, it is believed that this energy balance is not adequate, either due to the decrease in food intake (very frequent when there are swallowing problems), and the decrease in physical activity produced by alterations in mobility, or by structural damage (hypothalamic, mitochondrial) produced by the neurodegeneration process per se. When the energy balance is negative (energy expenditure> caloric intake), due to a decrease in intake or due to sustained involuntary physical activity (chorea), it can lead to the use of other energy substrates such as adipose tissue and muscle, triggering sarcopenia, cachexia, and ultimately, accelerating the neurodegeneration process. Weight loss and a low body mass index (BMI) in patients with neurodegenerative diseases lead to a greater development of neurological symptoms, while a high food intake has been associated with a more rapid progression in the symptoms of these patients. For all these reasons, it seems that nutrition plays a determining role, the dietary and nutritional analysis being fundamental.

To date, there are very few studies on energy balance in neurodegenerative diseases, addressing it from a comprehensive point of view and analysing each of its contributing components (energy expenditure-caloric intake). A better knowledge of the energy balance in HD may lead to the development of non-pharmacological, easily accessible and cost-effective therapeutic strategies such as lifestyle modifications, through adequate physical activity and nutritional intake.

02

Conditions studied

  • Huntington Disease

Browse trials for

Keywords

  • energy expenditure
  • physical activity
  • nutrition
  • wereables
  • daily life activity
03

In context

Huntington Disease

285 studies on the registry are indexed under Huntington Disease; 49 are open to participants now.

This study's enrollment of 30 is below the median of 90 across 78 observational studies indexed under Huntington Disease.

Browse Huntington Disease studies →

Lead sponsor

Hospital Universitario de Burgos is the lead sponsor of 3 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

People with Huntington's disease and non-gene family relatives

Inclusion criteria

  • Older than 18 years-old
  • Genetic confirmation of Huntington's disease
  • Symptomatic (motor manifestations with a score greater than 4 on the Unified HD scale)
  • Walk with minimal support
  • Participate in Enroll study
  • Non-gene carriers, family relatives

Exclusion criteria

Exclusion Criteria:

  • Sensory deficits or other systemic diseases which according to the Investigator judgment may interfere with the execution of the study
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
30 participants (actual)
Patient registry
No

Groups and cohorts

  • Case

    Patients with genetic confirmation of Huntington's disease, symptomatic (motor manifestations with a score greater than 4 on the Unified HD scale), who can walk with minimal support, without sensory deficits or other systemic diseases an Investigator judgment that may interfere with the execution of the study, coming from the Enroll study.

    Other: observational tests in face-to-face visit

  • Control

    Age, gender-matched non-gene carriers family relatives

    Other: observational tests in face-to-face visit

Interventions

  • Otherobservational tests in face-to-face visit

    All necessary evaluations will be carried out for data collection. Also, that same day, the investigators will give the device to participants for the 7-day home assessment

06

What researchers measure

Primary outcomes

  1. Measurement of energy expenditure at rest

    by indirect calorimetry recording respiratory exchange (Medisoft Ergocard, Medisoft Group, Sorinnes, Belgium)

    Time frame: 10 minutes

  2. Measurement of energy expenditure due to physical activity

    using a wearable device (Fitbit Charge), which allows quantification in a valid and reliable way, in patients with HD

    Time frame: 45 minutes

  3. Determination of caloric intake

    by registering eating habits (SUN food frequency questionnaire and a 3-day food diary)

    Time frame: 30 minutes

  4. Bone densitometry (DXA)

    Determination of body composition

    Time frame: 10 minutes

Secondary outcomes

  1. Validation of the wearable comparing the results with a gold standard

    using indirect calorimetry and accelerometery (ActiGraph wGT3X-BT) during activities of various kinds and intensity (walking at different speeds and slopes) on a treadmill (h / p / cosmos pulsar, h / p / cosmos sports and medical GMBH, Nussdorf-Traunstein, Germany) and activities of daily living together with pedalling on a cycle ergometer

    Time frame: 45 minutes

  2. Determination of the incidence of thermogenesis on energy expenditure and on the appearance of fatigue

    by recording the central and peripheral temperature (VitalSense, Phillips Respironics, Bend, OR, USA).

    Time frame: 2 hours

  3. Determination of lifestyle and weekly energy expenditure

    for this the participants will wear the device for 7 consecutive days

    Time frame: 7 days

07

Study locations

1 site
  • Hospital Universitario de Burgos
    Burgos, 09006, Spain
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05250323
Lead sponsor
Hospital Universitario de Burgos
Collaborators
La Caixa Foundation, Universidad Isabel I
Responsible party
Esther Cubo (Dr. Neurology, Hospital Universitario de Burgos) — Principal investigator
First posted
Feb 22, 2022
Start date
May 14, 2021
Primary completion
Jun 23, 2021
Completion
Jun 23, 2021
Last update
Feb 22, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion