NCT07250568 Office Program Effects on Pain, Posture, Muscle Physiology, Stress, Ergonomics, and Quality of Life in LBP Workers
| NCT ID | NCT07250568 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Suci Wahyu Ismiyasa |
| Condition | Low Back Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2026-03-23 |
| Primary Completion | 2026-06-17 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2026-03-23 with a primary completion date of 2026-06-17.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: 1. Identified LBP 2. Age between 18 - 60 years old 3. In the office, working in front computer/laptop minimum along 4 hours per day 4. Able to ambulate independently with or without walking aids 5. Controlled comorbidity e.g. DM, HPT, managed asthma and controlled thyroid conditions Exclusion Criteria: 1. Recumbent 2. Cancer, spinal fracture, neurological disorder (stroke, PBI and soon) 3. Participation in a current fitness program designed to prevent LBP recurrence 4. Spinal operation within the last six months 5. Pregnant 6. Medication (steroid therapy, non-steroidal anti-inflammatory drugs (NSAIDs), opioids, muscle relaxants, antidepressants or anxiolytics) 7. Insufficient to finish outcome measurements and exercise program 8. Participants who do not attend 3 consecutive weeks or 8 consecutive times
Contact & Investigator
Suci Wahyu Ismiyasa, M.Erg
PRINCIPAL INVESTIGATOR
Universiti Teknologi Mara
Frequently Asked Questions
Who can join the NCT07250568 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 58 Years, studying Low Back Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07250568 currently recruiting?
Yes, NCT07250568 is actively recruiting participants. Contact the research team at suciwahyuismiyasa@gmail.com for enrollment information.
Where is the NCT07250568 trial being conducted?
This trial is being conducted at Depok, Indonesia.
Who is sponsoring the NCT07250568 clinical trial?
NCT07250568 is sponsored by Suci Wahyu Ismiyasa. The principal investigator is Suci Wahyu Ismiyasa, M.Erg at Universiti Teknologi Mara. The trial plans to enroll 60 participants.