Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT06731361

Improved Prescribing for Older Nursing Home Patients

Led by Amsterdam UMC, location VUmc · Updated on 2024-12-12

450

Participants Needed

7

Research Sites

63 weeks

Total Duration

On this page

Sponsors

A

Amsterdam UMC, location VUmc

Lead Sponsor

Z

ZonMw: The Netherlands Organisation for Health Research and Development

Collaborating Sponsor

AI-Summary

What this Trial Is About

Research aim: To investigate the effect of training health care professionals in medication assessments on the medication use of nursing home residents with a limited life expectancy (\< 1.5-2 years). The core of the training is to tailor medication use to (palliative) treatment goals of nursing home residents. Design: A cluster randomized controlled trial on long term care wards in nursing homes, with the nursing home care organisations as unit of randomisation. The investigators intent to include 6 organisations and 450 nursing home patients. The research starts in september and lasts 1 year and 3 months. Eligible patients are nursing home patients of 65 years and older with a limited life expectancy (\< 1.5-2 year) of long term care wards. Intervention: The intervention includes a method in which healthcare professionals (medical practitioner, pharmacist and care worker) are trained to tailor medication to the (palliative) treatment goals of nursing home patients with a limited life expectancy. The training consists of 2 components: 1) medication assessment, and 2) advance care planning (ACP). In the intervention group, healthcare professionals receive the training in combination with supporting tools and educational materials, in the control group care continues as normal. The allocation ratio for control and intervention groups is 1:1. A process evaluation will take place simultaneously with the intervention study. Data collection takes place before the start of the intervention (T0), after 6 months (T1) and after 12 months (T2). Outcome measures: The primary outcome measure is potential under- and over-treatment with medication. The secondary outcome measure is experienced involvement in decision-making (measured with a short questionnaire based on the revised PATD (patients' attitude towards deprescribing)). Tertiary outcome measures are: quality of life, deaths, falls, hospital admissions/acute first aid referrals and pain. Discussion: The intervention is expected to result in a decrease in chronic and preventive medication prescriptions, an increase in medication for symptom treatment and more involvement (and satisfaction) of the nursing home resident in decision-making, without adverse effects.

CONDITIONS

Official Title

Improved Prescribing for Older Nursing Home Patients

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Nursing home patients aged 65 years and above
  • Living in long-term care wards in nursing homes
  • Resident in a long-term care ward for at least 4 weeks before study start
Not Eligible

You will not qualify if you...

  • Temporary nursing home patients (such as those in geriatric rehabilitation or hospice care)
  • Life expectancy less than 4 weeks
  • Life expectancy clearly more than 1.5 to 2 years (for example, patients with Huntington's disease)

AI-Screening

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Trial Site Locations

Total: 7 locations

1

Zorggroep Apeldoorn, location Randerode, De Hofstede and De Windkanter

Apeldoorn, Gelderland, Netherlands, 7334DV

Active, Not Recruiting

2

Zorggroep Noordwest-Veluwe, locaties Weideheem en de Arcade

Harderwijk, Gelderland, Netherlands, 3844 JW

Active, Not Recruiting

3

Cordaan, location Nieuw Vredenburgh

Amsterdam, North Holland, Netherlands, 1057 DZ

Actively Recruiting

4

Amaris, Location Alporti and Rubina

Hilversum, North Holland, Netherlands, 1215 SE

Active, Not Recruiting

5

AxionContinu, location Isselwaerde and de Schutse

IJsselstein, Utrecht, Netherlands, 3401 BN

Actively Recruiting

6

Zorgspectrum, location de Plataan

Vianen, Utrecht, Netherlands, 4133 GX

Actively Recruiting

7

Dignis, location de Veldspaat

Groningen, Netherlands, 9743XV

Active, Not Recruiting

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Research Team

M

Marlies Dijk, MD

CONTACT

E

Eefje Sizoo, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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