Fecal Incontinence Clinical Trial
— EPSPFIOfficial title:
Effect of an Educational Program for Staff in Nursing Homes Concerning Patients Fecal Incontinence: a Cluster-randomized Controlled Trial
| Verified date | January 2017 |
| Source | Norwegian University of Science and Technology |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Fecal incontinence (FI) has an increasing prevalence in the geriatric population which
cannot be explained by co-morbidity or anatomical and psychological changes of aging alone.
In the nursing home population previous studies suggest a prevalence between 10 and 69%, but
is most often reported to be between 40 and 55%. FI leads to a high direct and indirect
economic burden to the health-care system, and is an important cause og institutionalization
of the elderly patients. In addition, FI is associated with shame, social isolation and
reduced quality of life.
The importance of identifying treatable causes of FI in the frail elderly, rather than just
managing passively, is strongly emphasized. It is indicated that the level of awareness
among health personnel regarding appropriate assessment and treatment options is limited,
and that FI is considered a normal part of aging.
This study is based on the assumption that FI among nursing home patients can be prevented,
cured or ameliorated by offering nursing home staff knowledge of best practise. The primary
objective of the study is to test the hypothesis that a multifaceted educational program for
staff on assessment and treatment of FI, is associated with a reduction in patients'
frequency of FI.
The design of the study is a two armed cluster randomized trail (C-RCT) with a repeated
cross-sectional approach.The results will be analysed according to multilevel and
longitudinal modelling, and the study will use mixed effect models with the cluster treated
as a random effect.
| Status | Completed |
| Enrollment | 300 |
| Est. completion date | August 2015 |
| Est. primary completion date | July 2015 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | N/A and older |
| Eligibility |
Inclusion Criteria: Nursing homes with similar: - patients characteristcs - care staff/patients ratio - general practitioner consultancy Patients: - All patients on long term care residency (residency >month) Registered Nurses/authorized social educators: - All working half time or more Exclusion Criteria: Nursing homes: - With some kind of speciality (eks rehabilitation, dementia) Patients: - Short term care residency Registered nurses/authorized social educator: - Working less than half time - Working only night shifts |
| Country | Name | City | State |
|---|---|---|---|
| Norway | Sor Trondelag University College | Trondheim |
| Lead Sponsor | Collaborator |
|---|---|
| Norwegian University of Science and Technology | Norwegian Nurses Organisation |
Norway,
Blekken LE, Nakrem S, Gjeilo KH, Norton C, Mørkved S, Vinsnes AG. Feasibility, acceptability, and adherence of two educational programs for care staff concerning nursing home patients' fecal incontinence: a pilot study preceding a cluster-randomized controlled trial. Implement Sci. 2015 May 23;10:72. doi: 10.1186/s13012-015-0263-8. — View Citation
Blekken LE, Vinsnes AG, Gjeilo KH, Mørkved S, Salvesen Ø, Norton C, Nakrem S. Effect of a multifaceted educational program for care staff concerning fecal incontinence in nursing home patients: study protocol of a cluster randomized controlled trial. Trials. 2015 Mar 1;16:69. doi: 10.1186/s13063-015-0595-3. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in frequency of fecal incontinence among patients | As measured by The Long-Term Care Facilities Assessment System (interRAI-LTCF 2012), section H: Continence. Because of relatively high risk of death and movement out of clusters, a repeated cross-sectional opproach to analyses will be used. Frequency of FI will thereby be analysed on a across-sectional group level. | Baseline, after 3 months and after 6 months | |
| Secondary | Remission of fecal incontinence among patients | For remission of FI a cohort approach to data analyses with only those identified with FI at baseline and still present at 3 and 6 month follow-up, will be included in the analyses | Baseline, after 3 months and after 6 months | |
| Secondary | Change in knowledge among registered nurses and authorized social educators | Measured my a multiple choice test | Baseline, after 3 months and after 6 months | |
| Secondary | Change in FI-related concerns among patients | Relevant concerns as measured by The Long-Term Care Facilities Assessment System (interRAI-LTCF 2012) are: Mood and behavior, psycho-social wellbeing, urinary continence, constipation, diarrhea, skin condition, participation in activities | Baseline, after 3 months and after 6 months | |
| Secondary | Correlates of FI among patients | Relevant correlates as measured by The Long-Term Care Facilities Assessment System (interRAI-LTCF 2012) are: cognitive functioning, communication and vision, functionality and mobility, medical diagnosis, mouth and nutrition status, medications, treatment, examination/procedures | Baseline, after 3 months and after 6 months | |
| Secondary | Change in behavior among health personnel | Measured by analyses of patient assessments and interventions as documented by health personnel in the electronic patient record and by the Fecal Incontinence in Nursing Home Patients questionnaire | Baseline, after 3 months and after 6 months |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT03825575 -
Sacral Neuromodulation as Treatment for Fecal Incontinence
|
N/A | |
| Completed |
NCT00605826 -
A Randomized, Blinded, Multicenter Study to Evaluate NASHA/Dx for the Treatment of Fecal Incontinence
|
N/A | |
| Withdrawn |
NCT02208258 -
Efficacy, Safety, and Performance Study of a Novel Device Designed to Manage Fecal Incontinence in Hospitalized Bedridden Patients With Liquid to Semi-formed Stool.
|
N/A | |
| Completed |
NCT01957969 -
French Post-Inscription Study on Sacral Neuromodulation in the Treatment of Fecal Incontinence
|
N/A | |
| Completed |
NCT01939821 -
A Pilot Study to Evaluate Educational Programs to Improve Fecal Incontinence Care in Nursing Homes
|
N/A | |
| Completed |
NCT01710579 -
Normal Values in Ano-rectal 3D High Resolution Manometry
|
N/A | |
| Recruiting |
NCT00530933 -
Tibial Nerve Stimulation for Faecal Incontinence
|
N/A | |
| Completed |
NCT00565136 -
Evaluation of Outcomes of Restoring Pelvic Floor Support With TOPAS in Women With Moderate Fecal Incontinence Symptoms
|
Phase 1/Phase 2 | |
| Withdrawn |
NCT00522691 -
Efficacy of Sacral Nerve Stimulation Before Definitive Implantation
|
N/A | |
| Completed |
NCT00677508 -
Development of an Instrument to Measure Quality of Life in Children With Chronic Constipation and Soiling
|
||
| Completed |
NCT05032534 -
Examination of a New Irrigation System for Transanal Irrigation in Children With Fecal Incontinence
|
N/A | |
| Completed |
NCT05058326 -
Severity of Fecal Incontinence and Manometric Values Using the Anopress® Device in Women
|
||
| Completed |
NCT03746834 -
NASHA/Dx as a Perianal Implant for the Treatment of Persistent Fecal Incontience After Anorectal Malformation
|
Phase 4 | |
| Completed |
NCT00124904 -
Biofeedback for Fecal Incontinence
|
N/A | |
| Completed |
NCT03028636 -
LIBERATE - PRO: Eclipseâ„¢ System Registry
|
||
| Completed |
NCT04097288 -
Effects of Single Dose Citalopram and Reboxetine on Urethral and Anal Closure Function on Healthy Female Subjects
|
Phase 1 | |
| Completed |
NCT05621629 -
Management of FI After Surgery of ARM
|
||
| Withdrawn |
NCT04138602 -
BTL Emsella Chair Versus Sham for the Treatment of Fecal Incontinence
|
N/A | |
| Completed |
NCT03252951 -
Physical Therapy for Anal Incontinence
|
N/A | |
| Completed |
NCT04478799 -
Transcutaneous Posterior Nerve Stimulation inTreatment of Fecal Incontience
|
N/A |