e-Health Education Program at Workplace

Not Applicable

Completed

• Conditions: Health Behavior

• Registration Number: NCT02980237
• Lead Sponsor: Rosimeire Simprini Padula

Brief Summary

The objective this study is evaluate if an e-Health education program at the workplace to contributes to improve quality of life from Office Workers. And:Life style modification; Improve physical activity Reduces on Anthropometric Measures; Reduces Pain and discomfort in the musculoskeletal system

Detailed Description

Objective: The purpose of this study is evaluate the effectiveness of an e-Health education program at the workplace in the quality of life promotion.

Design: Double Blinded. Randomized clinical trial by cluster. Setting: Office Workers of the Universidade Publica do Estado da Bahia, Bahia State, Brazil. Participants: 348 office workers are enrollment, both sex, with over 18 year old.

Intervention: Participants will randomized in: (1) reference group will receive an e-learning health education compose by nine video-class according to the dimensions: 1) musculoskeletal health, 2) eating health e 3) mental health. A video will available by moodle platform every 20 days during six months. In this period the workers will monitored regarding to access the videos and and reinforcements to remain in the program. (2) intervention group: they will receive e-health education program with additional support healthcare tutor everyday.

Study Timeline

• Study First Submitted: 2016-08-23
• Study First Submitted QC: 2016-11-29
• Study First Posted: 2016-12-02
• Study Start: 2017-04-20
• Primary Completion: 2017-10-17
• Study Completion: 2018-03-02
• Status Verified: 2019-04
• Last Update Submitted: 2019-04-16
• Last Update Posted: 2019-04-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 384

Inclusion Criteria

• Technical-administrative workers, computer users for a minimum period of six months. ,
• Signed informed consent form

Exclusion Criteria

• Suspected or confirmed pregnant workers at randomization time
• Mothers what Breastfeeding
• Workers in annual leave.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change from baseline Quality of life at 6 and 8 months	Baseline, 6 and 8 months	A questionnaire to evaluate the improve the quality of life after 6 and 8 months after began the program will be used (WHOQOL-BREF :instrument comprises 26 items, which measure the following broad domains: physical health, psychological health, social relationships, and environment).

Secondary Outcome Measures

Name	Time	Method
Change from Lifestyle at 6 and 8 months	Baseline, 6 and 8 months	Change in health behavior, in physical activity level (min/week) after starting the eHealth program in 6 and 8 months will be measured.
Change from Anthropometric measure at 6 and 8 months	Baseline, 6 and 8 months	Changes on anthropometric measurements (weight, abdominal circumference, waist circumference, hip circumference, body mass and height). For this study, body mass index (BMI), body fat percentage (BFP) and waist-hip ratio will be used and assessment 6 and 8 months after starting the eHealth program.
Change from Pain and/or musculoskeletal discomfort measure at 6 and 8 months	Baseline, 6 and 8 months	To assessement the intensity of musculoskeletal complains (pain and discomfort) in baseline and 6 and 8 months an after starting the eHealth program.

Trial Locations

Locations (1)

Rosimeire Simprini Padula; 🇧🇷 Atibaia, SP, Brazil