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Spot Reduction in Male Adults

M

Molde University College

Status

Completed

Conditions

Healthy

Treatments

Other: Abdominal aerobic endurance exercise
Other: Control training intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05794854
MUCSR12

Details and patient eligibility

About

Spot reduction, referring to local body fat reduction, pertains to subcutaneous adipose tissue utilization from specific body parts during exercise. Its existence has been keenly debated, although generally accepted not to occur during exercise. However, it is based on not only equivocal data - commonly the training protocol typically applied is based on strength rather than endurance training. The investigators sought to test this assumption by utilizing endurance based exercise controlling for energy expenditure and using dual x-ray absorptiometric measures to assess body composition before and after training.

Enrollment

16 patients

Sex

Male

Ages

30 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • males
  • ≥ 30 years old
  • classified as overweight (Body mass index ≥ 25 kg ∙ m-2)
  • not participating in regular physical training

Exclusion criteria

  • < 30 years old
  • Body mass index < 25 kg ∙ m-2
  • participating in regular physical training

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

16 participants in 2 patient groups

abdominal aerobic endurance exercise
Experimental group
Description:
Subjects were combining treadmill running at 70% HRmax (27 minutes) with 4x4minutes (30-40% maximal strength, 1RM) of torso rotation and abdominal crunches (57 minutes), 4 d per wk for 10 weeks
Treatment:
Other: Abdominal aerobic endurance exercise
Control group
Active Comparator group
Description:
Subjects performed only treadmill running (45 minutes) at 70% HRmax for 4 d per week for 10 weeks.
Treatment:
Other: Control training intervention

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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