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Clinical Trials/NCT04290910
NCT04290910CompletedNot 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 enrollmentStarted: January 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
43
Locations
1
Primary Endpoint
Body Weight Loss

Study 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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Arms & Interventions

Weight Loss Program

Experimental

Single arm, all participants receive the weight loss program

Intervention: Weight Loss Program (Behavioral)

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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dylan MacKay

Assistant Professor

University of Manitoba

Study Sites (1)

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