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Clinical Trials/NCT01876095
NCT01876095CompletedNot Applicable

Discontinuing Inappropriate Medication in Nursing Home Residents (the DIM NHR Study): a Cluster Randomized Controlled Trial

University of Groningen1 site in 1 country992 target enrollmentStarted: June 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
992
Locations
1
Primary Endpoint
Successful medication discontinuation

Study Overview

Brief Summary

Nursing home residents are among the frailest patient groups with a high number of co-morbidities and a high use of medicines. Inappropriate polypharmacy (i.e. often overprescribing) is one of the major problems in the nursing home population increasing the number of adverse drug reactions, falls, hospital admissions, mortality as well as having an impact on health care utilization. Multidisciplinary medication reviews have a great potential to reduce inappropriate medication use. The purpose of this study is to determine the efficacy of a multidisciplinary medication review model focussing on discontinuing inappropriate medication in a cluster randomized controlled trial in 600 nursing home residents. The primary outcome measure is the difference in proportion of residents who successfully discontinued medication between intervention and control group after four months. Secondary outcome measures will be the drug burden index, adverse drug withdrawal events related to the discontinued medication, death, referral to hospitals and quality of life.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Nursing Home Wards:
  • •Inclusion criteria:
  • •Long stay ward
  • •Capability and commitment to perform a multidisciplinary multistep medication review.

Exclusion Criteria

  • •Short stay, revalidation or observation wards
  • •Specialized ward where patients with an atypical etiology are cared for.
  • •Elderly care physicians who have recently received or who are to receive recertification at short notice with regard to systematic medication review methodology.
  • •Participation in other studies aimed at improving the quality of drug prescription (in the past 12 months).
  • •Nursing Home Residents:
  • •Inclusion criteria:
  • •A life expectancy of >4 weeks as judged by the treating elderly care physician.
  • •IC provided by patients themselves or provided by a legal representative for incapacitated patients.
  • •Exclusion criteria:
  • •Refusal of treatment with medicines.
  • •Having received a multidisciplinary systematic medication review in the past 6 months.
  • •Being terminally ill and having a life expectancy ≤ 4 weeks as judged by the treating elderly care physician.
  • •Other reasons at the discretion of the elderly care physician / nursing staff

Arms & Interventions

Multidisciplinary medication review

Experimental

The multidisciplinary medication review consists of 5 steps:

Step #1: Assessing patients' experiences and preferences regarding medicine use en assessing their medical history, allergies and lab results Step #2: Drug reviewing to assess contra-indicated medication and duplicate medication using consensus criteria e.g. START STOPP Beers criteria Step #3: Reflecting on results of drug reviewing Step #4: Setting up a pharmacotherapeutical action plan Step #5: Execution of pharmacotherapeutical action plan

Intervention: Multidisciplinary medication review (Procedure)

usual care

No Intervention

Includes medication safety monitoring and ad hoc medication reviews on clinical indication that differ in quality and frequency, but no standardized multidisciplinary multistep medication reviews in the way as described for the intervention arm

Outcomes

Primary Outcomes

Successful medication discontinuation

Time Frame: 4 months

The number of residents for whom ≥1 inappropriate medication(s) are succesfully discontinued i.e. without relapse or severe withdrawal effects

Secondary Outcomes

  • Hospital admission(4 months)
  • Falling(4 months)
  • number of visits to outpatient clinics / emergency rooms / by medical consultants(4 months)
  • Dose adjustment(4 months)
  • Death(4 months)
  • Safer alternative medication(4 months)
  • Bone fractures(4 months)
  • Drug burden index(4 months)
  • Quality of Life(4 months)
  • adverse drug withdrawal events(4 months)
  • Medication initiation(4 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Katja Taxis

Professor of Pharmacotherapy and Clinical Pharmacy

University of Groningen

Study Sites (1)

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