NCT02982408

Brief Summary

Low birth weight (LBW), a marker of impaired fetal growth is an independent and strong risk factor for type 2 diabetes (T2D). A western lifestyle characterized by a surplus of calories, and/or a low physical activity level, associated with increased fat storage and altered lipid metabolism plays a central role in the pathogenesis of insulin resistance and T2D. Using state-of-the-art large-scale integrative physiology studies combined with basic studies of adipose and muscle tissue stem cell functions, the investigators aim to determine if LBW individuals exhibit decreased subcutaneous adipose tissue expandability, postprandial hyperlipidaemia and ectopic fat accumulation when exposed to 4 weeks of carbohydrate overfeeding. The investigators will subsequently examine if exercise training can revert and/or minimize the deleterious effects of carbohydrate overfeeding in a possibly birth weight differential manner.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable type-2-diabetes-mellitus

Timeline
Completed

Started Aug 2016

Typical duration for not_applicable type-2-diabetes-mellitus

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

August 1, 2016

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

August 23, 2016

Completed
3 months until next milestone

First Posted

Study publicly available on registry

December 5, 2016

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2019

Completed
Last Updated

September 6, 2019

Status Verified

September 1, 2019

Enrollment Period

2.6 years

First QC Date

August 23, 2016

Last Update Submit

September 3, 2019

Conditions

Outcome Measures

Primary Outcomes (2)

  • Adipose tissue expandability

    Percent (%) subcutaneous, visceral adipose tissue and hepatic fat will be determined by MR scanning in the two groups

    baseline

  • Adipose tissue expandability

    Percent (%) subcutaneous, visceral adipose tissue and hepatic fat will be determined by MR scanning in the two groups

    Difference between the two groups at baseline, after 4 weeks overfeeding and after 12 weeks exercise training.

Secondary Outcomes (3)

  • Glucose turnover rate

    Baseline, 4 weeks overfeeding, 12 weeks training

  • Lipid turnover rate

    Baseline, 4 weeks overfeeding, 12 weeks training

  • Epigenetics

    Baseline, 4 weeks overfeeding, 12 weeks training

Study Arms (2)

Low birth weight (LBW)

EXPERIMENTAL

25 males born at term (weeks 39-41) in 1979-1981 with LBW (BW\<10th percentile)

Dietary Supplement: High carbohydrate overfeedingBehavioral: ExerciseBehavioral: Normal physical activity

Normal birth weight (NBW)

EXPERIMENTAL

25 BMI- and age-matched males born at term (weeks 39-41) with normal birth weight (NBW) control individuals (BW: 50-90th percentile)

Dietary Supplement: High carbohydrate overfeedingBehavioral: ExerciseBehavioral: Normal physical activity

Interventions

All participant's individual energy requirement will be determined in mega joules (MJ) per day. The energy requirement will be multiplied by a factor 1.5 for a low physical activity level (PAL). The MJ will be rounded up or down to the nearest whole number. The participant will receive food corresponding to \~25% additional energy above their calculated energy requirement. The 25% extra energy will be supplied to the participants for 4 weeks in the form of food containing simple carbohydrates. The subjects will be given a daily snack package containing processed foods or refined foods such as sweets, cookies, soft drinks, juice etc. To ensure an adequate energy surplus (i.e. weight gain), physical activity has to be decreased to a low level during the 4 weeks overfeeding period.

Low birth weight (LBW)Normal birth weight (NBW)
ExerciseBEHAVIORAL

Half of the participants will be randomized to a 3-month exercise-training program. The training program consists of combined aerobic training and strength training. The training program is performed unsupervised 3 times per week 45 minutes per session for 3 months in the local fitness center. Before engaging in the training program a maximal oxygen consumption test (VO2 max) are conducted and the maximal heartrate (HR) are determined.Participants are wearing the Polar V800 HR monitor and are asked to note their HR in a training log at the end of the last interval at each training session. The strength training program consist of 6 exercises (2 exercises paired together) involving the large muscle groups. The first training session is completed supervised at Rigshospitalet . After 6 weeks the training program is adjusted. Compliance will be ensured by phone calls, text messages and e-mails from study personnel.

Low birth weight (LBW)Normal birth weight (NBW)

The other half of the participants will be randomized to a 3-month with normal physical activity level (control). The participants will have to return to the physical activity level they had before entering the study (baseline level). Compliance will be ensured by phone calls and text messages from study personnel. The subjects will wear a simple pedometer on the hip showing the number of steps. Once a week a text message (SMS-track) is automatically sent asking the participants to enter the weekly number of steps. The test personnel receive the reply and contact the participant if the number of steps does not match the baseline level. During the first and the last 7 days of the exercise intervention participants are wearing 2 accelerometers measuring their physical activity behavior.

Low birth weight (LBW)Normal birth weight (NBW)

Eligibility Criteria

Age35 Years - 40 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • without known disease (approved health examination)
  • caucasian
  • born at term (weeks 39-41) in Denmark
  • recruited from the national Danish Birth Registry
  • born with either low or normal birthweight (see previous)

You may not qualify if:

  • family history of diabetes in two generations (1st and 2nd degree relatives)
  • self-reported high physical activity level (\>10hrs /week).
  • weight loss/gain \>3 kg within the past 6 months
  • alcohol intake of more than general recommendations
  • substance abuser
  • intake of medication know to affect outcomes

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rigshospitalet, Denmark

Copenhagen, Capital Region, 2100, Denmark

Location

MeSH Terms

Conditions

Diabetes Mellitus, Type 2Insulin ResistanceDyslipidemias

Interventions

Exercise

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesHyperinsulinismLipid Metabolism Disorders

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Charlotte Brøns, PhD

    Rigshospitalet, Denmark

    PRINCIPAL INVESTIGATOR
  • Allan Vaag, PhD, DMsc

    Rigshospitalet, Denmark

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

August 23, 2016

First Posted

December 5, 2016

Study Start

August 1, 2016

Primary Completion

March 1, 2019

Study Completion

March 1, 2019

Last Updated

September 6, 2019

Record last verified: 2019-09

Locations