Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:30 PM
Ignite Modification Date:
2025-12-24 @ 10:30 PM
NCT ID:
NCT00665535
Eligibility Criteria:
Inclusion Criteria: Participants will:
* Be free of pressure ulcers upon admission to the study.
* Have a Braden Scale Score between 10 - 12 (high risk) or 13 -14 (moderate risk) within one week of admission (new residents) or greater than 90 days (established residents) of study participation
* Have a high-density foam replacement mattress in use or can be transferred to such a mattress.
* Are 65 years or older. Younger residents are present in fewer numbers and may have different health issues and co-morbidities than older residents.
* Can legally grant consent to participate or have available surrogates to grant consent. If able, participant should assent when a surrogate grants consent.
* Expected to have a length of stay of 21 days or greater.
Exclusion Criteria:
* Pressure ulcer is present upon initial examination.
* The Braden Scale score is 15 or greater indicating mild risk or no risk, or 9 or below indicating very high risk.
* The resident cannot be turned on 3 anatomical surfaces (side, back, side) or has a contraindication to repositioning.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
65 Years
Study:
NCT00665535
Study Brief:
Protocol Section:
NCT00665535