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Clinical Trials/NCT03904160
NCT03904160CompletedNot Applicable

Web-based Personal or Peer Group Weight Management Study

University of Turku1 site in 1 country109 target enrollmentStarted: January 4, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
109
Locations
1
Primary Endpoint
The number of participants who obtained and maintained a weight loss of at least 5% at 12 months

Study Overview

Brief Summary

The PERGROUP trial aims to investigate whether Web-based personal or Web-based group counselling weight management program can help to achieve lifestyle changes needed for weight loss and improvement in quality of life and cardiovascular risk factors. The control group is the traditional nurse-lead weight management group counselling.

Detailed Description

In this study, efficacy of two web-based weight management systems will be compared to a traditional nurse-lead sessions for weight management.

Ten nurse-lead group counselling sessions lasting 90 minutes each will be conducted in three groups of 10-14 participants. Each session comprise education about healthy diet, psychoeducation and discussions.

The web-based group counselling program offers informative weight management system with peer-based conversation possibility. Three groups of 10-14 participants who gather together for three nurse-lead sessions in the weeks 0, 5, and 12. The web-based program can be used for a year.

The web-based personal counselling program offers informative weight management system with conversation possibility with the nurse for 12 weeks. Altogether 37 participants are enrolled and they can use the web-based weight management system for one year.

In each intervention arm, intervention and counselling provided by the study nurses last for three months. Among all participants, weight loss, cardiometabolic data, information of lifestyle and quality of life will be measured at baseline, after the nurse-lead intervention (three months) and 12 months from the baseline.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Sequential
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •body mass index 25 kg/m2 or higher

Exclusion Criteria

  • •pregnancy
  • •active cancer
  • •acute cardiovascular event less than three months before
  • •untreated thyroid disease
  • •systematic corticosteroid medication
  • •anorexia or bulimia
  • •impaired communication ability

Arms & Interventions

Nurse-lead group

Sham Comparator

Nurse-lead sessions for weight management. Ten sessions lasting 90 minutes each in three groups of 10-14 participants. Each session comprise education about healthy diet, psychoeducation and discussions.

Intervention: Weight management (Behavioral)

Web-based group

Experimental

Web-based weight management system with peer-based conversation possibility. Three groups of 10-14 participants who gather together for three nurse-lead sessions in the weeks 0, 5, and 12. The web-based program can be used for a year.

Intervention: Weight management (Behavioral)

Web-based personal

Experimental

Web-based weight management system with conversation possibility with the nurse for 12 weeks. Altogether 37 participants who can use the web-based weight management system for one year.

Intervention: Weight management (Behavioral)

Outcomes

Primary Outcomes

The number of participants who obtained and maintained a weight loss of at least 5% at 12 months

Time Frame: From baseline to 12 months

The number of participants who obtained and maintained a weight loss of at least 5% at 12 months

Secondary Outcomes

  • Change in plasma triglycerides in mmol/l(From baseline to 12 months)
  • Change in weight in kilograms(From baseline to 12 months)
  • Change in body mass index.(From baseline to 12 months)
  • Change in plasma fasting glucose in mmol/l(From baseline to 12 months)
  • Work ability(From baseline to 12 months)
  • Change in diastolic blood pressure in mmHg(From baseline to 12 months)
  • Change in waist circumference in centimeters(From baseline to 12 months)
  • Change in plasma total cholesterol in mmol/l(From baseline to 12 months)
  • Change in plasma high-density lipoprotein cholesterol in mmol/l(From baseline to 12 months)
  • Change in plasma low-density lipoprotein cholesterol in mmol/l(From baseline to 12 months)
  • Overall quality of life measured by the Eurohis instrument(From baseline to 12 months)
  • Health-related quality of life measured with the EuroQol instrument.(From baseline to 12 months)
  • Change in systolic blood pressure in mmHg(From baseline to 12 months)
  • Change in body fat percentage(From baseline to 12 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Päivi Korhonen

Professor of General Practice

University of Turku

Study Sites (1)

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