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The effects of nurse-initiated early pain management program (NIEPMP) for acute back pain in Emergency Medicine Ward: A randomized control trial

The effects of nurse-initiated early pain management program (NIEPMP) for acute back pain in Emergency Medicine Ward: A randomized control trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002855
Enrollment
Unknown
Registered
2012-12-26
Start date
2010-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Acute Back Pain

Interventions

Intervention:Heat Therapy

Sponsors

NIL
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: i. Eligible participants should be older than 18 and are Hong Kong residents; ii. Patient who suffered from back pain with less than 4-week duration before presenting to the AED; iii. They were admitted to EMW after 5pm (after the service hour of physiotherapy) and waiting for physiotherapy next day; iv. They should be able to read, understand and communicate in Chinese (Cantonese); v. Signed informed consent after explanation.

Exclusion criteria

Exclusion criteria: i. Patients who presented to AED with back pain more than 4 weeks; ii. Patients who suffered from unstable spine, obvious orthopedic problems or lower limb weakness are being diagnosed by emergency physicians; iii. Patients who have previous spinal surgery, structural damage or gross structural defect of the spine; iv. Patients who have history of chronic LBP or LBP due to specific underlying pathology such as infection, tumor, osteoporosis, rheumatoid arthritis, fracture, inflammation, or musculoskeletal disease; v. Patients who were under the influence of alcohol or drug intoxication before admission to EMW; vi. Patients who were confused and mentally incapacitated; vii. Involvement in other experimental studies as other study treatments they received would affect the score on chosen instruments.

Design outcomes

Primary

MeasureTime frame
Disability;

Secondary

MeasureTime frame
Pain;Anxiety;Satisfaction;

Countries

China

Contacts

Public ContactYau Ching Ying
yaucy04@yahoo.com.hk+852 94648430

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026