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Can an independent consultation and feedback program for patients and surgeons help to optimize decisions on which materials are used for joint replacement surgeries?

Smartphone and web-based independent consultation and feedback for joint replacement surgeries: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10152297
Enrollment
1000
Registered
2020-01-08
Start date
2020-12-31
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Hip or knee joint replacement surgery Surgery

Interventions

The study utilizes a quasi-RCT design involving patients needing joint replacement surgery and the corresponding orthopedic surgeons selected, from hospitals of Anhui province, randomized into equal i
while the control arm receives routine medical services. The intervention consists of two main components targeting patients and doctors. For patients, the interventio

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Surgeons: 1. All orthopedic surgeons from the selected hospitals are encouraged to participate in this study Patients: 1. Awaiting hip or knee joint replacement surgery 2. Have the ability to communicate and make independent decisions 3. Aged 18 years or older

Exclusion criteria

Exclusion criteria: 1. Patients unwilling to participate in the study 2. Patients with previous experience of hip or knee joint replacement surgeries 3. Patients unable to communicate clearly and/or make independent decisions

Design outcomes

Primary

MeasureTime frame
1. Quality-of-life assessed using the EQ-5D-5L scale at 6 months, 12 months and 18 months after discharge 2. Cost of medical materials assessed using questionnaire custom-designed for this study at 6 months after discharge These data will be used to calculated cost-effectiveness.

Secondary

MeasureTime frame
1. Peer expert audit score assessed using a custom-designed questionnaire at 6 months after discharge 2. Quality control inspection score assessed using a custom-designed questionnaire at 6 months after discharge 3. Patient awareness rate (treatment schedule, surgical risk, material selection, etc) assessed using a custom-designed questionnaire at discharge, and 6 months, 12 months and 18 months after discharge 4. Patient satisfaction assessed using a custom-designed questionnaire at discharge and 6 months after discharge 5. Total medical expense assessed using a custom-designed questionnaire at 6 months after discharge

Countries

China

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 23, 2026