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Pressure Ulcer Prevention and Care for Community Bedridden Patients: A Multi-Methods Study

Pressure Ulcer Prevention and Care for Community Bedridden Patients: A Multi-Methods Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260401013
Enrollment
136
Registered
2026-04-01
Start date
2025-04-02
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Pressure ulcers among community-dwelling bedridden patients, including elevated risk of pressure ulcer development and limited caregiver competence in pressure ulcer prevention and care Community care

Interventions

Participants in the standard care group received standard ward nursing care, including turning every 2 hours, skin inspection , and use of standard mattresses and so on,Participants assigned to the co
(2) a WeChat support group for theoretical guidance and timely communication
(3) risk-tailored follow-up based on Braden scores, high risk weekly, moderate risk biweekly, low risk every four weeks, delivered via WeChat, phone, or home visits by supervised medical student volun
(4) individualized adjustments to address barriers such as low nighttime repositioning adherence or limited access to pressure-relieving equipment.
Standard Care Group,Multi-component pressure ulcers prevention intervention
standard community based prevention care

Sponsors

Youjiang Medical University for Nationalities
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.aged 18 years or older; 2. long-term bedridden status, defined as continuous bed rest for at least 3 months and spending more than 8 hours per day in bed or using a wheelchair; 3.no PUs at baseline; 4.residence in a community within Baise City; and 5.provision of written informed consent by the patient or their legally authorized representative.

Exclusion criteria

Exclusion criteria: 1. inability or unwillingness of patients or family members to cooperate with home-based PUs prevention education; 2.medical contraindications to repositioning; 3.receipt of palliative care; 4. severe cognitive impairment precluding informed consent or participation in study procedures; 5.transfer from the community to hospital care due to acute illness or critical conditions during the study period.

Design outcomes

Primary

MeasureTime frame
Pressure ulcers incidence 30 days after the intervention was completed European Pressure Ulcer Advisory Panel (classification system

Secondary

MeasureTime frame
Pressure ulcers risk 30 days after the intervention was completed Braden Scale,Caregiver knowledge pressure ulcersregarding prevention 30 days after the intervention was completed Chinese version of the Knowledge Assessment Instrument for Pressure Ulcer Preventio,Caregiving ability 30 days after the intervention was completed Chinese version of the Caregiver Task Inventory

Countries

China

Contacts

Public ContactSamoraphop Banharak

Please provide to Khon Kaen University, Thailand

sbanharak@kku.ac.th6643202407

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026