Actively Recruiting
Office Program Effects on Pain, Posture, Muscle Physiology, Stress, Ergonomics, and Quality of Life in LBP Workers
Led by Suci Wahyu Ismiyasa · Updated on 2025-11-26
60
Participants Needed
1
Research Sites
18 weeks
Total Duration
On this page
Sponsors
S
Suci Wahyu Ismiyasa
Lead Sponsor
P
Pembangunan Nasional Veteran Jakarta University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This interventional study aims to evaluate the effectiveness of an office worker's program in reducing low back pain and improving physical and psychosocial outcomes among office employees. The primary objective is to determine the effects of the intervention on pain, lumbar posture, muscle physiology (including core stability, flexibility, fatigue, and endurance), ergonomics, stress levels, and quality of life across different intervention groups. Participants will be assigned to one of three groups: Group 1: Exercise program, posture education, and standing advice Group 2: Posture education and standing advice Group 3: standing advice only The study will compare outcomes between groups to identify which combination of interventions provides the greatest benefits for office workers with a tendency to experience low back pain.
CONDITIONS
Official Title
Office Program Effects on Pain, Posture, Muscle Physiology, Stress, Ergonomics, and Quality of Life in LBP Workers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Identified low back pain
- Age between 18 and 60 years old
- Working in an office using a computer or laptop for at least 4 hours per day
- Able to walk independently with or without walking aids
- Controlled comorbidities such as diabetes, hypertension, managed asthma, and controlled thyroid conditions
You will not qualify if you...
- Being bedridden
- Having cancer, spinal fracture, or neurological disorders such as stroke or brain injury
- Currently participating in a fitness program to prevent low back pain recurrence
- Spinal surgery within the last six months
- Pregnancy
- Taking medications like steroids, NSAIDs, opioids, muscle relaxants, antidepressants, or anxiolytics
- Unable to complete study measurements or exercise program
- Missing 3 consecutive weeks or 8 consecutive sessions of the program
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Universitas Pembangunan Nasional Veteran Jakarta
Depok, West Java, Indonesia, 16514
Actively Recruiting
Research Team
S
Suci Wahyu Ismiyasa
CONTACT
Z
Zarina Zahari, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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