The Impact of Multisensory Compensation Position Training on Patients Undergoing Vitrectomy and Filling Operation: A Clinical Randomized Controlled Trial

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2600117896

Enrollment

Unknown

Registered

2026-01-29

Start date

2026-02-15

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Rhegmatogenous Retinal Detachment (RRD,Epiretinal Membrane (ERM),Macular Hole (MH)

Interventions

Control group:The standard postural care protocol, carried out by the study interventionists, included the following: 1. Use of a prone positioning pillow made for post-vitrectomy recovery

2. Providing postoperative home care education on proper positioning and preventing complications

3. Offering follow-up assistance through a WeChat-based nursing service.

Intervention Group (Multi-sensory compensation Training group):Based on routine positional care, the research interventionists implemented a multisensory positional management protocol for vitrectomy

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. It meets the international diagnostic criteria for rhegmatogenous retinal detachment, epiretinal membrane and macular hole. 2. Age >=18 years old and =7 days. 5. No impairment of smell, hearing or touch; 6. No physical movement disorders.

Exclusion criteria

Exclusion criteria: 1. Allergic to the components of the Chinese herbal sachet or experiencing discomfort upon smelling it; 2. Accompanied by other ocular diseases such as glaucoma or cataract; 3. Old retinal detachment; 4. Presence of psychiatric or cognitive impairment; 5. Suffering from severe cardiovascular or cerebrovascular disease preventing compliance with prone positioning; 6. Illiterate and lacking access to smart mobile devices; 7. Currently participating in another interventional study.

Design outcomes

Primary

Measure	Time frame
Score of anxiety;	—

Secondary

Measure	Time frame
Score of comfort;Time of face down position;Best Corrected Visual Acuity;Retinal reattachment ;closure of retinal breaks;Intraocular pressure;	—

Countries

China

Contacts

Public ContactDeng Chaohua

Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology

dengch@hust.edu.cn+86 158 0270 9534

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026