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Status unknownNCT02175810Updated May 11, 2018

Impact of Bariatric Surgery on Cardiorespiratory Function

An observational study in Obesity, Bariatric Surgery Candidate and Physical Activity, sponsored by St George's, University of London. Status unknown at 1 site in United Kingdom. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2018-05-11.

Sponsored by St George's, University of London · Observational

The sponsor has not verified this record recently (last verified May 2018), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
24
Ages
18 Years to 50 Years
Sex
All
01

Study summary

Obesity is a growing problem worldwide and its prevention has become one of the leading priorities for the World Health Organisation. Obesity results from chronic imbalance between energy intake and energy expenditure. Although early prevention of obesity is preferable, surgical treatment is often required for severely obese people.

Bariatric surgery has been shown to be the most effective therapy for severe obesity. Weight loss following bariatric surgery results in significant improvements in coexisting comorbidities, such as diabetes and hypertension but there is controversy whether bariatric surgery also improves aerobic capacity.

The purpose of this study is to investigate the effects of bariatric surgery on cardiopulmonary function and on daily physical activity. It is hypothesized that bariatric surgery will improve aerobic capacity and result in beneficial lifestyle changes from sedentary to more active.

02

Conditions studied

  • Obesity
  • Bariatric Surgery Candidate
  • Physical Activity

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Keywords

  • Obesity
  • Bariatric surgery
  • physical activity
  • cardiopulmonary exercise test
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,692 are open to participants now.

This study's planned enrollment of 24 is below the median of 135 across 1,283 observational studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

St George's, University of London is the lead sponsor of 105 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with scheduled bariatric surgery at St George's Healthcare NHS Trust.

Inclusion criteria

  • Ages 18 years to 50 years
  • Patients enrolled in the bariatric surgery program of St George's Hospital with BMI > 40 kg/m2, or 35-40 kg/m2 in the presence of other obesity-related comorbidities such as hypertension or type- 2 diabetes

Exclusion criteria

Exclusion Criteria:

  • Locomotor difficulties which would prevent participants from completing the cardiopulmonary exercise testing
  • Weight > 190 kg (due to weight restrictions of equipment used to transfer patients in the event of medical emergencies)
  • Cognitive impairment
  • Patients unable to follow instructions in English
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
24 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Cardiorespiratory function assessed by peak oxygen consumption (VO2peak)

    Time frame: One to two weeks before surgery and six months after surgery

Secondary outcomes

  1. Lung function

    Lung function will be assessed by spirometry and body plethysmography

    Time frame: One to two weeks before surgery and six months after surgery

  2. Heart function

    Echocardiography will be performed to assess heart function.

    Time frame: One to two weeks before surgery and six months after surgery

  3. Inspiratory muscle strength

    Maximal inspiratory pressure and sniff nasal pressure will be recorded.

    Time frame: One to two weeks before surgery and six months after surgery

  4. Peripheral muscle strength

    Maximum isometric strength of hand/ forearm, quadriceps and hip flexors muscles will be evaluated

    Time frame: One to two weeks before surgery and six months after surgery

  5. Free living sedentary and physical activity times

    Daily physical activity habits will be assessed by an accelerometer and International Physical Activity Questionnaire: Long (IPAQ-Long). Participants will be required to wear the accelerometer for four consecutive days during the two study points.

    Time frame: One to two weeks before surgery and six months after surgery

07

Study locations

1 of 1 sites recruiting
  • St George's Healthcare NHS Trust
    London, SW17 0RE, United Kingdom
    • Dimitra Nikoletou · Contact · dinikole@sgul.ac.uk · +44 20 8725 5647
    • Emma R McGlone · Sub investigator
    • Ommar A Khan · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 11, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02175810
Lead sponsor
St George's, University of London
Collaborators
Universidade Federal do Triangulo Mineiro, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
Responsible party
Sponsor
First posted
Jun 26, 2014
Start date
Jun 2014
Primary completion
Oct 2018 (estimated)
Completion
Oct 2018 (estimated)
Last update
May 11, 2018

Study contacts

Dimitra Nikoletou, PhD
Contact
dinikole@sgul.ac.uk
+44 20 8725 5647
Marcia S Volpe
principal investigator · Universidade Federal Triangulo Mineiro
Dimitra Nikoletou
study chair · Kingston University and St George's University of London
Marcus Reddy
study director · St George's Healthcare NHS Trust

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2018. You cannot join it, but the record below documents what was studied.

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