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e-Health Education Program at Workplace

Effectiveness of an e-Health Program at Workplace in the Promotion of Quality of Life of Office Workers: Protocol of a Randomized Controlled Trial by Cluster

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02980237
Acronym
e-Health
Enrollment
384
Registered
2016-12-02
Start date
2017-04-20
Completion date
2018-03-02
Last updated
2019-04-17

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

Conditions

Health Behavior

Keywords

Office workers, Quality of life, e-Learning, Occupational health

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.

Interventions

OTHEReHealth_additional support

An e-learning education program whose audiovisual content will be implemented. Nine audiovisual e-Health program will be composed of nine video classes addressing the following topics: 1) musculoskeletal health, 2) healthy diet and 3) mental health were identified through focus group. A communication tool will be adopted is the Moodle environment. All the participants will be able to whipping the web platform and questions regarding access and navigation are answered by e-mail. All participants will be monitored, as viewing the videos, and whenever it is identified that the participants not accessed and lack of interest of reasons. A team of tutors will be responsible for online support providing reinforcing stimuli and clarifying any questions (intervention group) on the content.

OTHEReHealth_program

The comparative group will receive the same eHealth education program that intervention group. But the comparative group will receive only audiovisuals without additional support. .

Sponsors

Rosimeire Simprini Padula
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline Quality of life at 6 and 8 monthsBaseline, 6 and 8 monthsA 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

MeasureTime frameDescription
Change from Anthropometric measure at 6 and 8 monthsBaseline, 6 and 8 monthsChanges 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 monthsBaseline, 6 and 8 monthsTo assessement the intensity of musculoskeletal complains (pain and discomfort) in baseline and 6 and 8 months an after starting the eHealth program.
Change from Lifestyle at 6 and 8 monthsBaseline, 6 and 8 monthsChange in health behavior, in physical activity level (min/week) after starting the eHealth program in 6 and 8 months will be measured.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026