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Clinical Trials/NCT01939821
NCT01939821
Completed
N/A

A Pilot Study to Evaluate Feasibility of Educational Programs With Regard to Good Fecal Incontinence Care in Nursing Homes

Norwegian University of Science and Technology1 site in 1 country60 target enrollmentSeptember 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Fecal Incontinence
Sponsor
Norwegian University of Science and Technology
Enrollment
60
Locations
1
Primary Endpoint
The proportion patients assessed by the clinical guidelines
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The investigators are planning to do a cluster randomized trial to test the effect of different educational programs for staff according to nursing home patients FI (fecal incontinence). Since there are very few published trials of treatment of FI in older people, and no rigorously evaluated studies on interventions for FI in nursing homes, or rigorously evaluated continence education program for staff concerning continence care, a pilot study is necessary. The aim for the pilot study is to evaluate feasibility, acceptability and adherence according to the educational intervention, methods used and outcome measures. This is designed to be an external pilot study. External pilot studies are small scale versions of the main study which are not intended to be part of the main study. The pilot intervention period is 3 month.

Registry
clinicaltrials.gov
Start Date
September 2013
End Date
April 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Nursing homes Wards with 24 hour long term care residency, similar nurse/patient ratio and General Practitioner consultancy, comparable patient groups according to frailty, comparable ward size according to number of patients and staff.
  • Patients All patients on long term residency (1 month or more) are eligible for measurements.
  • Registered nurses (RN) and authorized social educators (ASE) RN's and ASE's with position above 50% are eligible according to participation in the educational meeting and to be recruited as a local opinion leader in intervention
  • All staff is invited to the educational outreach meetings throughout the intervention period.

Exclusion Criteria

  • Nursing homes with diverse staff and patient composition
  • Patients on short term residency
  • Registered nurses (RN) and authorized social educators (ASE) RN's and ASE's with position less than 50%

Outcomes

Primary Outcomes

The proportion patients assessed by the clinical guidelines

Time Frame: 3 months

90% of the patients assessed by the clinical guideline

Secondary Outcomes

  • Proportion of completed patient health questionnaires(3 months)
  • Acceptable performance of multiple choice test measuring change in staff knowledge.(3 months)
  • The proportion of missing data in each completed questionnaire(3 months)

Study Sites (1)

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