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Web-based Personal or Peer Group Weight Management Study

Web-based Personal or Peer Group Weight Management Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03904160
Acronym
PERGROUP
Enrollment
109
Registered
2019-04-05
Start date
2018-01-04
Completion date
2019-03-30
Last updated
2020-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Risk Factors, Overweight and Obesity, Quality of Life, Work Ability

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.

Interventions

BEHAVIORALWeight management

Please see the arm descriptions.

Sponsors

University of Turku
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
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

Design outcomes

Primary

MeasureTime frameDescription
The number of participants who obtained and maintained a weight loss of at least 5% at 12 monthsFrom baseline to 12 monthsThe number of participants who obtained and maintained a weight loss of at least 5% at 12 months

Secondary

MeasureTime frameDescription
Work abilityFrom baseline to 12 monthsThe percentage of participants in whom weight management intervention will be associated with participants´ Work Ability Score (WAS). The total score range is 0 to 10 with higher value representing better work ability.
Overall quality of life measured by the Eurohis instrumentFrom baseline to 12 monthsThe number of participants in whom weight management intervention will be associated with quality of life assessed by the Eurohis instrument. Mean change from baseline in frequencies of reported problems will be reported.
Health-related quality of life measured with the EuroQol instrument.From baseline to 12 monthsThe number of participants in whom weight management intervention will be associated with quality of life assessed by the EuroQol instrument. Mean change from baseline in frequencies of reported problems will be reported.
Change in systolic blood pressure in mmHgFrom baseline to 12 monthsChange in systolic blood pressure in mmHg
Change in waist circumference in centimetersFrom baseline to 12 monthsChange in waist circumference in centimeters
Change in weight in kilogramsFrom baseline to 12 monthsChange in weight in kilograms
Change in diastolic blood pressure in mmHgFrom baseline to 12 monthsChange in diastolic blood pressure in mmHg
Change in body fat percentageFrom baseline to 12 monthsChange in body fat percentage
Change in plasma total cholesterol in mmol/lFrom baseline to 12 monthsChange in plasma total cholesterol in mmol/l
Change in plasma high-density lipoprotein cholesterol in mmol/lFrom baseline to 12 monthsChange in plasma high-density lipoprotein cholesterol in mmol/l
Change in plasma low-density lipoprotein cholesterol in mmol/lFrom baseline to 12 monthsChange in plasma low-density lipoprotein cholesterol in mmol/l
Change in plasma triglycerides in mmol/lFrom baseline to 12 monthsChange in plasma triglycerides in mmol/l
Change in plasma fasting glucose in mmol/lFrom baseline to 12 monthsChange in plasma fasting glucose in mmol/l
Change in body mass index.From baseline to 12 monthsChange in body mass index. Weight and height will be combined to report body mass index in kg/m2

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026