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Effects of Exercise Training on Cognitive Function and Neurotrophic Factors in Overweight Adults

Effects of High Intensity Interval- vs Resistance or Combined- Training for Improving Cognitive Function and Neurotrophic Factors in Overweight Adults (BrainFit Study): Factorial Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02915913
Acronym
BrainFit
Enrollment
60
Registered
2016-09-27
Start date
2016-09-30
Completion date
2016-12-31
Last updated
2018-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Function, Motor Activity, Obesity

Brief summary

The BrainFit Study aims to examine acute effects of High Intensity Interval- vs Resistance or Combined program has benefits on Cognitive Function as well as on secretion and regulation of neurotrophic factors or neurotrophins in a cohort of sedentary, overweight adults (aged 18-30 years) from Bogota, Colombia.

Interventions

BEHAVIORALExperimental: High Intensity Interval

Walking on a treadmill 4min at 80-90% peak heart rate and recovery 4 min at 65% peak heart rate until expenditure of 500 kcal

BEHAVIORALResistance training

Completing a resistance circuit (including upper and lower muscle groups) as many times as needed according to subject weight until expenditure of 500 kcal

Walking on a treadmill as intervention 1 until 50% the energy expenditure prescribed is reached, then completing a resistance circuit until 100% energy expenditure is reached

This group will receive the usual clinical care according to the consensus recommendations of the national goals for cardiovascular health promotion and disease reduction of the American Heart Association and Colombian guidelines COLDEPORTES.

Sponsors

Universidad del Rosario
CollaboratorOTHER
Universidad Nacional de Colombia
CollaboratorOTHER
Universidad Santo Tomas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Written informed consent. * Interested in improving health and fitness. * Central obesity: waist circumference ≥90cm * Body mass index ≥ 26 kg/m(2)

Exclusion criteria

* Systemic infections. * Weight loss or gain of \>10% of body weight in the past 6 months for any reason. * Currently taking medication that suppresses or stimulates appetite. * Uncontrolled hypertension: systolic blood pressure 160 mm Hg or diastolic blood pressure 95 mm Hg on treatment. * Gastrointestinal disease, including self-reported chronic hepatitis or cirrhosis, any episode of alcoholic hepatitis or alcoholic pancreatitis within past year, inflammatory bowel disease requiring treatment in the past year, recent or significant abdominal surgery (e.g., gastrectomy). * Asthma. * Diagnosed diabetes (type 1 or 2), fasting impaired glucose tolerance (blood glucose 118 mg/dL), or use of any anti-diabetic medications. * Currently taking antidepressant, steroid, or thyroid medication, unless dosage is stable (no change for 6 months). * Any active use of illegal or illicit drugs. * Current exerciser (\>30 min organized exercise per week). * Indication of unsuitability of current health for exercise protocol (PARQ).

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Brain-derived neurotrophic factorBaseline and 60 minutes immediately after the interventions endsMeasurement of serum Brain-derived neurotropic factor true blood samples.

Secondary

MeasureTime frameDescription
Change from Baseline in Neurotrophin-3Baseline and 60 minutes immediately after the interventions ends
Change from Baseline in Neurotrophin-4Baseline and 60 minutes immediately after the interventions ends
Change from Baseline change in Cognitive FunctionBaseline and 60 minutes immediately after the interventions endsCognitive Performance Test (BPT) computerized cognitive assessment battery developed by Lumos Labs, Inc.

Countries

Colombia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026