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Clinical Trials/NCT04290910
NCT04290910
Completed
Not Applicable

A Pilot Study Evaluating the Clinically Managed Weight Loss Program At the Wellness Institute At Seven Oaks General Hospital

University of Manitoba1 site in 1 country43 target enrollmentJanuary 1, 2019
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
University of Manitoba
Enrollment
43
Locations
1
Primary Endpoint
Body Weight Loss
Status
Completed
Last Updated
last year

Overview

Brief Summary

This is a pilot study evaluating a clinically managed weight loss program. The program consists of a 17-week weight loss program which involves a multidisciplinary team where personalized interventions are given to participants from the team based on the participants goals.

Detailed Description

The clinically managed weight loss program is managed by a clinical team including a Program Manager, Registered Dietitians, Canadian Society of Exercise Physiology-Certified Personal Trainers, Clinical Psychology Associate or Cognitive Behavioural Therapist, and a Physician. The team will collaborate together to prescribe a plan best suited for the participants' needs with the focus on lifestyle changes, such as, sleep, mental health, and behaviours. Outcome measures will be collected as part of the pilot study, such as, anthropometric measurements and body composition, cardiovascular assessment, clinical chemistry, physical activity, nutrition, and behaviour and health screening questionnaires.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
June 1, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dylan MacKay

Assistant Professor

University of Manitoba

Eligibility Criteria

Inclusion Criteria

  • Participant is willing and able to give informed consent for participation in the trial.
  • Male or female, aged 18 years or above.
  • Are overweight or obese (BMI over 24.9)

Exclusion Criteria

  • Female participant who is pregnant or lactating.

Outcomes

Primary Outcomes

Body Weight Loss

Time Frame: 4 months

Weight will be measured in kg to the nearest 0.1 kg using a InBody 570 scale

Secondary Outcomes

  • Changes in Quality of Life(4 months)
  • Changes in Sleep Quality(4 months)

Study Sites (1)

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