Skip to content

Feasibility analysis and evaluation of remote monitoring of family rehabilitation of patients with back pain based on digital medical platform

Feasibility analysis and evaluation of remote monitoring of family rehabilitation of patients with back pain based on digital medical platform

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051234
Enrollment
Unknown
Registered
2021-09-16
Start date
2021-12-31
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

low back pain

Interventions

Group 1:DTx system managed patient
Group 2:Paper handouts managed patient

Sponsors

Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Software Supervision Team: (1) The gender of the patient is not limited, age: 18-65 years old; (2) Outpatient and inpatient patients with low back pain symptoms; (3) The smartphone can be used normally, or the accompanying family members can assist in using it; (4) No mental or cognitive impairment; (5) Understand the nature of the research and be willing to sign the informed consent. 2. Manual Mission Team: (1) The gender of the patient is not limited, age: 18-65 years old; (2) Outpatient and inpatient patients with low back pain symptoms; (3) No mental or cognitive impairment; (4) Understand the nature of the research and be willing to sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Software Supervision Team: (1) Malignant tumors of the spine, infections, spinal deformities and other diseases; (2) Unable to accept radiological inspection; (3) Severe osteoporosis, cardiovascular and cerebrovascular diseases; (4) Unable to cooperate in completing all research steps and contents; (5) Severe bleeding tendency or coagulation dysfunction; (6) Pregnant or lactating women. 2. Manual Mission Team: (1) Malignant tumors of the spine, infections, spinal deformities and other diseases; (2) Unable to accept radiological inspection; (3) Severe osteoporosis, cardiovascular and cerebrovascular diseases; (4) Unable to cooperate in completing all research steps and contents; (5) Severe bleeding tendency or coagulation dysfunction; (6) Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
pain index;Oswestry Disability Index Questionnaire;

Countries

China

Contacts

Public ContactYu Yan

Department of Spine Surgery, Tongji Hospital

yyu15@tongji.edu.cn+86 21 66111706

Outcome results

None listed

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