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Development of pillow and therapeutic exercise for computer users with nonspecific neck pain

Development of pillow and therapeutic exercise for computer users with nonspecific neck pain

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200526002
Enrollment
Unknown
Registered
2020-05-26
Start date
2019-05-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Computer users with non&#45

Interventions

The participants will be asked to sleep on the commercialized pillow for 30 minutes&#44
3 days a week for 6 weeks.,The participants will be asked to sleep on the newly designed pillow for 30 minutes&#44
3 days a week for 6 weeks.,Participants of this group receipted self&#45
mobilization at the 2nd and the 5th of the cervical spinous process level with the elastic brand while active resistance neck exercise.It took 30 minutes to exercise 3 days/ week for 6 weeks
Experimental Other,Experimental Other,Experimental Other
A commercialized pillow group ,A Newly designed pillow group,Self&#45
mobilization with neck exercise group

Sponsors

Graduate School, Khon Kean University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
26 Years to 40 Years

Inclusion criteria

Inclusion criteria: -A daily computer user with constantly or frequently for at least 5 days/week every week occurring computer-related neck pain for more than 1 year. -They had worked on a computer for at least 3 years. -Working with computer continuous for at least 4 hr./day. -They had experienced neck pain in the previous 7 days, and self-reported pain intensity of at 3–5 on a scale of 0–10 and not take oral medicine for relieving pain.

Exclusion criteria

Exclusion criteria: -Having been on sick leave for more than 1 month during the last year. -They had accident or surgery at head, neck, and arms within 6 months prior to the study. -They had experienced pain in more than three body regions. -A medical history of cardiovascular or cerebrovascular accident, hypertension, fibromyalgia, rheumatoid arthritis, cervical disc herniation or spinal cord compression, whiplash, malignancy, vertebrobasilar insufficiency, and other serious chronic diseases. The researcher has access to the participant's medical history from the history taking and participants who provide treatment information and medical examination for the researcher by themselves. -Recent fracture of spine and arms within 6 months prior to the study from the history taking. -Loosening joints/ joint instability of the spine and arms from the history taking. -Upper limb muscle weakness caused by neurological involvement from the history taking. -Pregnancy. -Performing more than 2 h per week of vigorous physical exercise. -They had experienced neck pain for fewer than 8 days in the last 1 year.

Design outcomes

Primary

MeasureTime frame
Functional ability 1st visit, after the first intervention, and after 6 weeks Neck disability index

Secondary

MeasureTime frame
Pain 1st visit, after the first intervention, and after 6 weeks Visual analog scale ,Cervical range of motion 1st visit, after the first intervention, and after 6 weeks CROM instrument,Heart rate variability 1st visit, after the first intervention, and after 6 weeks Heart rate variability instrument,Neck muscle strength 1st visit, after the first intervention, and after 6 weeks Maximal isometric neck extension by a digital scale,Occiput to wall distance 1st visit, after the first intervention, and after 6 weeks Vernier caliper,Tissue hardness and Pressure pain threshold of the upper trapezius muscle 1st visit, after the first intervention, and after 6 weeks Tissue hardness algometer combo

Countries

Thailand

Contacts

Public ContactPanida Chaiming

Khon Kaen University

panida_ch@hotmail.com+66843312541

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026