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Effects of Health Education for Patients Received Minimally Invasive Lumbar Spinal Surgery

T

Taipei Medical University

Status

Unknown

Conditions

Lumbar Degenerative Disease
Low Back Pain

Treatments

Behavioral: Perioperative Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT04120532
N201904001

Details and patient eligibility

About

Lumbar degenerative disease surgery has been a routine clinical operation, and has good treatment effects. Although the patient's neurological symptoms improve after surgery, many patients still have postoperative muscle soreness. The postoperative rehabilitation intervention for the patients receiving traditional lumbar surgery has been confirmed to effectively improve pain and disability. However, in recent years, minimally invasive lumbar spinal surgery has gradually replaced traditional surgery, postoperative pain has been greatly reduced. Therefore, patients have the opportunity to receive early intervention in rehabilitation, but there is no standardization process for rehabilitation of minimally invasive lumbar spine surgery. Therefore, this study aims to establish a health education program for patients receiving minimally invasive lumbar spinal surgery, and conduct clinical trials to test its effectiveness.

Enrollment

100 estimated patients

Sex

All

Ages

45 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 45 and 90 years old.
  • Low back pain has been persisting at least 3 months.
  • Clinical degeneration diagnosis supports the need of MI-TLIF.
  • Able to understand Chinese.

Exclusion criteria

  • Emergency surgery.
  • Unstable vital sign.
  • Any psychological, neurological, orthopedics, cardiopulmonary, and cancer history.
  • Had spinal surgery before.
  • Pregnancy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Education group
Experimental group
Treatment:
Behavioral: Perioperative Rehabilitation
Usual care group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Chiao-Ling Chen, Master

Data sourced from clinicaltrials.gov

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