Obesity Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Healthcare units such as NHS services and nursing homes that voluntarily choose to take part and provide direct patient care
- Units that agree to follow evidence-based guidelines on hand hygiene, plus at least one of these topics: pain, urinary incontinence, obesity prevention, breastfeeding, smoking cessation, falls prevention, or pressure injury prevention
- People of any age who may experience pain and are receiving care in a hospital, nursing home, or primary care setting
- People aged 18 or older who have stress, urge, or mixed urinary incontinence, and who have been admitted for at least 7 days or can continue care for up to around 6 weeks
- Babies and children up to 12 years old in good general health, where the focus is on obesity prevention (children aged 2–12 must not have been overweight or obese in the year before the study baseline)
- People who are breastfeeding, healthy newborns born after 36 weeks of pregnancy weighing at least 2,500 grams, and their supporting partners or family members, during the first 6 months of the baby's life
- People aged 18 or older who currently smoke, where the focus is on smoking cessation
- Adults aged 18 or older who are in a hospital, nursing home, or home care programme and are considered at risk of developing pressure injuries
- Adults aged 65 or older, and adults aged 18 or older who may have walking difficulties due to neurological or traumatic conditions, medication effects, muscle weakness, or drowsiness, where the focus is on falls prevention
- All health professionals caring for patients in participating units, in relation to the hand hygiene component of the study
Who may not be able to join:
- No exclusion criteria were listed in the official trial documentation (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: María Teresa Moreno-Casbas, PhD, Instituto de Salud Carlos III
Phone: 644617184
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
ICU beds with alcohol-based preparations at the point of care; Hospital beds with alcohol-based preparations at the point of care; Consumption of alcohol-based preparations in Primary Care centers; Consumption of alcohol-based preparations in hospital units without admission; Consumption of alcohol-based preparations in Nursing Homes.; Detection of pain at admission; Pain related to a procedure likely to cause pain; Pain after a change in the patient's clinical situation; Pain intensity assessment; Comprehensive pain assessment; Pain management care plan; Patient or/and caregiver education on...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.