ClinicalTrials.gg
Active, not recruitingNCT05991609Updated Feb 10, 2025

Extreme Morphology and Metabolic Health

An observational study in Skeletal Dysplasia, sponsored by University of Bath. Active, not recruiting at 1 site in United Kingdom. Open to participants aged 16 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-02-10.

Sponsored by University of Bath · Observational

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year 1 month ago, but the record still lists the study as active, not recruiting.

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Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
102
Ages
16 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 22 studies in Mucopolysaccharidosis IV with a site in United Kingdom — 6 open to participants now, 7 under way, 1 of them phase 3. Mucopolysaccharidosis IV · United Kingdom.

Started
2023
with 1 other
Observational
6 of 22
1 open now
Registered
16th of 22
by date
Lead sponsor
1 of 22
University of Bath

Among the 22 studies in Mucopolysaccharidosis IV with a site in United Kingdom, this one is one of 2 that started in 2023, is one of 6 observational ones, and was the 16th registered.

Mucopolysaccharidosis IV

101 studies on the registry are indexed under Mucopolysaccharidosis IV; 27 are open to participants now.

Browse Mucopolysaccharidosis IV studies →

Open to participants now

6 of the 22 studies in Mucopolysaccharidosis IV with a site in United Kingdom are open now. Recruiting first, the newest first:

1 more — sign in →

All 6 open studies →

A study can be open while its sites in United Kingdom have not opened yet or have stopped. Only those recruiting at a site in United Kingdom →

Who these studies take

Of the 20 Mucopolysaccharidosis IV studies recruiting now, 9 (45%) set no upper age limit and 7 (35%) stop at 75 or younger; 15 take children under 18; 7 take healthy volunteers.

This study: 16 Years and older · all sexes · healthy volunteers too.

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 22 studies in Mucopolysaccharidosis IV with a site in United Kingdom, or all of them as a file.
02

Study summary

Researchers at the University of Bath are investigating the metabolism of individuals with extreme body size, including those with skeletal dysplasia (commonly known as dwarfism), to manage health risks such as heart disease. By better understanding how body size could change how the body processes food, or how being bigger or smaller may influence eating habits, healthy living guidelines to tackle issues such as obesity and overweight in these populations can be improved. With help from expertise in the psychology field, this research will also investigate whether the mental health of these individuals has been affected by their size. On the whole, this study will involve one 24-hour visit to a research laboratory at the University of Bath, followed by a 2-week monitoring period to capture 'normal' physical activity and eating routines.

Read the detailed description

After signing informed consent to take part in the study, participants will be asked to complete a health entry criteria questionnaire, including a physical activity readiness questionnaire and Eating Disorder Examination Questionnaire, to confirm eligibility. Participants will also be required to complete a health questionnaire for administration of anaesthetic as part of the biopsy procedure. Individuals who are very small or very big (without skeletal dysplasia) will be asked to attend the laboratory for a pre-trial screening as an additional eligibility criterion. This will involve measuring height, body mass, and standing on a specialised scale (bioelectrical impedance scale) which estimates how much muscle and fat someone has. If it is suspected that the participant meets the stated fat-free mass criteria, a complete a full body Dual Energy X-ray Absorptiometry (DEXA) scan to assess body composition more accurately will be completed. This involves lying flat on a bed for \~7 minutes and resting whilst the scan takes place. The research team will then inform the participant after analysing the scan results if they are eligible and can continue with the study.

All participants deemed eligible who are able and willing to take part will be invited to attend the University of Bath Human Physiology Laboratory for the full trial.

On day 1, prior to attending the University of Bath participants will be asked to eat a standardised diet of a cereal breakfast, and a supermarket purchased sandwich, drink and snack meal deal for lunch, with self-selected quantities. Participants will ideally be fasted for 4-5 hours before arrival (\~17:00).

Upon arrive at the University, individuals with skeletal dysplasia will also be asked to complete the health entry criteria questionnaire and physical activity readiness questionnaire to ensure eligibility. It is important that participants let the researchers know of any medical conditions or any change in circumstance since signing up. All information is strictly confidential.

The research team will first take measurements of height, body mass, waist and hip circumference, abdomen diameter (distance from your front to back), sitting height and blood pressure. Early into the visit, participants will also be briefed on collecting urine into provided containers. Individuals with skeletal dysplasia will then have a Dual Energy X-ray Absorptiometry (DEXA) scan to assess body composition. All participants will also have a Peripheral Quantitative Computed Tomography (pQCT) scan which involves placing one leg into a round scanner to assess the tissues in your leg e.g., bone, muscle and fat (as if the image were a slice). The scan requires you to keep your leg still for \~10 minutes.

Participants will then be asked to rest in a bed and relax. In a seated position, participants will complete a lung function test at rest which requires blowing into a specialised device through a mouthpiece. Following this, after lying down and being briefed on the procedure, a trained member of staff will take a fat tissue biopsy from the abdomen to analyse genes and proteins in the cells. The fat biopsy involves inserting a needle with suction just below the skin to extract the cells and will be performed under local anaesthetic. This procedure may cause a bruise for up to 7 days. Following on from this, a muscle biopsy will be taken from the quadriceps (large muscle on the front of the thigh) to again measure genes and proteins as well as signalling pathways involved in our metabolism. The needle is inserted just inside the muscle and 2/3 snips of tissue are collected. The research team will provide information and equipment for aftercare of the biopsy sites to prevent infection after participants leave the laboratory.

Participants will then be provided with a hot meal for dinner. This will be a standard portion of Sainsbury's Love Your Veg! Lentil Cottage Pie (400 g, serves 1). Prior to turning the lights out at 22:00, participants will be fitted with sleep monitoring kit known as polysomnography. The equipment includes an abdominal and chest pressure sensing band, a nasal cannula and some sticky sensors placed directly on the skin.

On the morning of day 2, a researcher will wake the participant at 07:00. Using a mouthpiece (alike to a snorkel) and nose clip, expired air at rest will be collected for 20 minutes to calculate how much energy is burnt at rest. Participants will also be asked to give a breath sample into a small glass tube through a straw (this is related to a tracer method explained below). Body mass will be measured again after the participant has an opportunity to use the bathroom.

Once settled back in bed, a trained member of staff will insert a cannula (small plastic tube) into a vein on the back of the participant's hand or forearm. This will stay in place for the remainder of the day and allows repeated blood samples to be taken throughout the following tests. For participants with skeletal dysplasia, the genetic material found in cells will be taken out of the first blood sample and later analysed to confirm a correct diagnosis of achondroplasia. Participants will be asked to place the hand in a warm box set at 55°C which helps blood flow and makes taking samples easier for the research team. All participants will then be asked to complete a series of appetite questions, a portion selection task, and blood pressure will be taken.

When the hand is warm and initial appetite tasks are completed, participants will be provided with a sugary drink and asked to finish it within 5 minutes. The drink will also contain a sugar tracer which is stable and safe-to-consume. This allows the research team to assess how the drink is being processed by the body in real time. For a few individuals from each 'subgroup' (achondroplasia, skeletal dysplasia, extremely large body size, and extremely small body size), a different tracer called acetate will be added to the drink which will help with some calculations of how the body processes the sugar. Blood samples (10 mL) will be drawn from the cannula every 15 minutes for the first hour, and 30 minutes for the next two hours. At these same intervals, the participant will be asked to blow into a small tube using a straw to assess the appearance of the tracer on the breath (an indicator of how much sugar is being burnt from the drink, as opposed to the body's sugar stores, hence the need for a baseline sample). Participants will also be asked to complete the appetite questions and portion selection task whenever a blood sample is drawn. At 60, 120 and 180 minutes, a one 5-minute sample of air will be collected just as upon waking, and blood pressure will be measured on the hour. In between samples the participant may also complete a series of questionnaires regarding mental health (optional).

At 11:00, participants will be presented with another appetite task and then a lunch meal (pesto pasta with cheese, and a glass of orange juice) to consume within 20-minutes. A few additional appetite questions will be asked pre- and post- meal consumption. The following 3 hours will be similar to before, with regular appetite scales to complete, and blood samples drawn every 15 minutes for the first hour, and 30 minutes for the next two hours. At 60, 120 and 180 minutes, one 5-minute breath sample and a smaller tracer breath sample through the straw will be collected, and blood pressure recorded.

Participants will then be asked to complete a short treadmill test to calibrate the activity monitor by wearing a heart rate monitor on a chest strap whilst walking. Five 3-minute incremental stages will be calculated based on the participants 'normal' self-selected walking speed. During the final minute of each stage, a one-minute breath sample will be collected and heart rate recorded. A breath sample into a tracer collection tube will also be obtained at the end of each exercise stage. Whilst on the treadmill, participants will be asked to describe how difficult the exercise stages feel. If the fastest speed has not exceeded 'hard' exercise, the researcher will ask if the participant feels able to complete a final stage at a higher intensity (not exceeding a rating of perceived exertion of 15) to assist calibration of the activity monitor. Within 30 seconds of finishing on the treadmill one final blood sample will be drawn from the cannula before removing it.

On leaving the lab, participants will be provided with an activity monitor, a motion watch, a food diary (either on a mobile app or paper copy), and food and body weight scales. A small device to continuously measure blood sugar levels will also be fitted to the back of the arm. The device is inserted with a very small needle which is then removed, leaving only the patch with a small probe in the arm. The research team will instruct participants on how to wear the activity monitor on the chest and ask that participant wear this at all times other than when swimming or bathing, and record food intake for 14-days. During this time, participants will be asked to weigh themselves first thing in the morning and last thing at night, as well as recording sleep times and quality.

03

Conditions studied

  • Skeletal Dysplasia

Keywords

  • Morphology
  • Skeletal dysplasia
  • Metabolism
04

Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Individuals with extreme body size or proportions.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 16 years or over
  • Any diagnosed form of skeletal dysplasia (i.e., extreme proportionate or disproportionate short stature)
  • Individuals without skeletal dysplasia but presenting with extreme body morphology, defined as: individuals with extreme large body morphology (males >75 kg fat-free mass and females >57.25 kg fat-free mass), or males and females with extreme small body morphology (\<47.4 kg fat-free mass).

Exclusion criteria

Exclusion Criteria:

  • Any reported condition, behaviour or reported use of substances which may pose undue personal risk to the participant or introduce bias into the study, except for any which are ubiquitous in society and so would be equally distributed between groups and/or therefore relevant to generalisation (e.g., statins, caffeine, GLP-1 agonists).
  • Females who are pregnant or lactating
  • Individuals with a diagnosed history of eating disorders (e.g., anorexia)
  • Individuals with known bleeding disorders (exclusion for only)
  • Individuals with known allergy or intolerance to lidocaine
  • Inability to read or speak English, or otherwise to consent to procedures
  • Individuals who are not weight stable (i.e., >3 kg change in body mass in past 3 months)
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
102 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Individuals with extreme body size

    Any individual with a form of skeletal dysplasia, or extremely small or large body size.

06

What researchers measure

Primary outcomes

  1. Glucose incremental area under the curve during the oral glucose tolerance test

    Difference in blood glucose incremental area under the curve between individuals with skeletal dysplasia, and extremely small and large body size.

    Time frame: 3 hours

Secondary outcomes

  1. Fasted blood glucose concentration

    Time frame: Baseline

  2. Fasted blood insulin concentration

    Time frame: Baseline

  3. Insulin response to oral glucose tolerance test

    Incremental area under the curve of blood insulin after oral glucose tolerance test

    Time frame: 3 hours

  4. C-Peptide response to oral glucose tolerance test

    Incremental area under the curve of blood C-Peptide after oral glucose tolerance test

    Time frame: 3 hours

  5. Regulatory hormone response to oral glucose tolerance test

    Incremental area under the curve of regulatory hormones e.g. ghrelin after oral glucose tolerance test

    Time frame: 3 hours

  6. Glycaemic response to mixed meal tolerance test

    Incremental area under the curve of blood glucose after mixed meal tolerance test

    Time frame: 3 hours

  7. Insulin response to mixed meal tolerance test

    Incremental area under the curve of blood insulin after mixed meal tolerance test

    Time frame: 3 hours

  8. C-Peptide response to mixed meal tolerance test

    Incremental area under the curve of blood C-Peptide after mixed meal tolerance test

    Time frame: 3 hours

  9. Regulatory hormone response to mixed meal tolerance test

    Incremental area under the curve of regulatory hormones e.g. ghrelin after mixed meal tolerance test

    Time frame: 3 hours

  10. Resting metabolic rate

    Time frame: Baseline

  11. Substrate oxidation during oral glucose tolerance test

    Total fat and carbohydrate oxidation

    Time frame: 3 hours

  12. Substrate oxidation during mixed meal tolerance test

    Total fat and carbohydrate oxidation

    Time frame: 3 hours

  13. Exogenous carbohydrate oxidation

    Time course for whole-body exogenous carbohydrate using stable isotope methodology

    Time frame: 7 hours

  14. Fasting muscle glycogen concentration

    Difference between individuals with skeletal dysplasia, extremely small and large body morphology.

    Time frame: Baseline

  15. Non-oxidative glucose disposal

    Difference in exogenous carbohydrate consumption and exogenous carbohydrate oxidation

    Time frame: 7 hours

  16. Continuous interstitial glucose concentration

    Time frame: 10 days

  17. Adipose tissue markers of insulin signalling

    Time frame: Baseline

  18. Adipose tissue markers of glucose metabolism

    Time frame: Baseline

  19. Skeletal muscle markers of insulin signalling

    Time frame: Baseline

  20. Skeletal muscle markers of glucose metabolism

    Time frame: Baseline

  21. Fasted concentration of systemic adipokines (e.g., adiponectin, resistin, leptin etc.)

    Time frame: Baseline

Other outcomes

  1. Height

    Metres

    Time frame: Baseline

  2. Body mass

    Kilograms

    Time frame: Baseline

  3. Change in body mass over 14 days of free-living monitoring

    Kilograms

    Time frame: 14 days

  4. Waist:Hip ratio

    Time frame: Baseline

  5. Sagittal abdominal diameter

    Centimeters

    Time frame: Baseline

  6. Blood pressure

    mmHg

    Time frame: 6 hours

  7. Intracellular markers and signalling pathways related to carbohydrate metabolism in adipose tissue

    Comparing adipose tissue between skeletal dysplasia, extremely small and large groups

    Time frame: Baseline

  8. Intracellular markers and signalling pathways related to carbohydrate metabolism in skeletal muscle

    Comparing muscle tissue between skeletal dysplasia, extremely small and large groups

    Time frame: Baseline

  9. Full blood lipid profile

    Blood analysed and compared between skeletal dysplasia, extremely small and large groups

    Time frame: 7 hours

  10. Fasted markers of chronic low-grade inflammation

    Blood analysed and compared between skeletal dysplasia, extremely small and large groups

    Time frame: Baseline

  11. FGFR protein expression and signalling pathway exploration

    Muscle tissue analysed and compared between skeletal dysplasia, extremely small and large groups

    Time frame: Baseline

  12. 24-hour protein oxidation

    Grams per minute

    Time frame: 24 hours

  13. Genotype- FGFR3 mutation (skeletal dysplasia group only)

    Assessed from buffy coat layer

    Time frame: Baseline

  14. Panel of female sex hormones

    To verify menstrual cycle phase

    Time frame: Baseline

  15. DEXA bone mineral density

    Time frame: Baseline

  16. DEXA fat mass

    Time frame: Baseline

  17. DEXA fat-free mass

    Time frame: Baseline

  18. pQCT - muscle cross-sectional area

    Time frame: Baseline

  19. pQCT - tissue density

    Time frame: Baseline

  20. pQCT - bone geometry

    Time frame: Baseline

  21. Assessment of eating behaviour

    The Three Factor Eating Questionnaire

    Time frame: Baseline

  22. Visual analogue scale appetite ratings

    Time frame: 6 hours

  23. Portion selection task

    Time frame: 6 hours

  24. Polysomnography profile

    Time frame: Baseline

  25. Daily self-reported energy intake during free-living monitoring

    Daily self-reported energy intake using Nutritics Libro Application

    Time frame: 14 days

  26. Daily free-living physical activity energy expenditure

    Daily free-living physical activity measured by Actiheart monitor

    Time frame: 14 days

  27. Free-living sleep quality

    Time frame: 14 days

  28. Free-living sleep duration

    Time frame: 14 days

  29. Free-living light exposure

    Time frame: 14 days

  30. Diet induced thermogenesis

    Calculated from self-reported energy intake

    Time frame: 14 days

  31. Heart rate during exercise

    Beats per minute

    Time frame: 15 minutes

  32. Rate of perceived exertion during exercise

    BORG scale

    Time frame: 15 minutes

  33. Energy expenditure during exercise

    Substrate oxidation during walking exercise

    Time frame: 15 mins

  34. Mental health assessment

    Validated questionnaires

    Time frame: Baseline

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2023 (actual). Primary completion is estimated for Sep 2025, 27 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 20, 2023
First posted
Aug 14, 2023
StartActual
Jun 17, 2023
Primary completionEst.
Sep 30, 2025
CompletionEst.
Sep 28, 2035
Last update
Feb 10, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 10, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05991609
Lead sponsor
University of Bath
Collaborators
University of Bristol
Responsible party
James Betts (Professor, University of Bath) — Principal investigator
First posted
Aug 14, 2023
Start date
Jun 17, 2023
Primary completion
Sep 30, 2025 (estimated)
Completion
Sep 28, 2035 (estimated)
Last update
Feb 10, 2025

Study contacts

James A Betts, PhD
principal investigator · University of Bath

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 active, not recruiting, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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