Skip to main content
Clinical Trials/NCT04242745
NCT04242745CompletedNot Applicable

The Effect of an Audible Alarm on the Fluid Consumption of The Elderly Living in a Nursing Home: A Randomized, Controlled Trial

Izmir Katip Celebi University1 site in 1 country100 target enrollmentStarted: July 27, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Fluid deficit of the elderly

Study Overview

Brief Summary

Research shows that older people need reminders to increase fluid consumption. The aim of the research was to investigate the effect of an audible alarm on the fluid consumption of old people living in a nursing home. The research was conducted as a single-blind, randomized controlled, prospective experimental study on the pre-test post-test model.

The study was performed between 27 July 2017 and 1 February 2018 at a nursing home in the west of Turkey. Out of 979 in nursing home who conformed to the inclusion criteria of the study, 100 (intervention group (n: 50) and control group (n: 50) were voluntarily included in the sample. The intervention group was given education and a wristwatch which gave an audible alarm to remind them to drink liquid, the control group was given only education. The old people in both groups were monitored before the education, after the education, after the audible alarm and 15 days after the audible alarm every three days on total of 12 days. The amount of liquid that the elderly should drink daily was determined according to Gaspar formula.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Criteria for inclusion in the study were being aged 65 or over, not having a fluid deficiency and living in nursing home.

Exclusion Criteria

  • •Exclusion criteria were having an education level of less than primary education
  • •Being visually or aurally impaired,
  • •Being bedridden,
  • •Not being able to take liquids orally, Having health problems such as fever,
  • •Vomiting, diarrhea or kidney disease causing fluid loss,
  • •Taking diuretic medication and using more than more than five doses per day,
  • •Having a diagnosis of a disease such as kidney failure or cardiac insufficiency requiring restriction of fluids, or having a diagnosis of neurological or psychiatric dysfunction, or dementia or Alzheimer's.

Arms & Interventions

Intervention group

Experimental

Procedure/Surgery:The intervention group was given education and a wristwatch which gave an audible alarm to remind them to drink liquid.

Intervention: Intervention group (Behavioral)

Intervention group

Experimental

Procedure/Surgery:The intervention group was given education and a wristwatch which gave an audible alarm to remind them to drink liquid.

Intervention: Control group (Behavioral)

Control group

No Intervention

The control group was given only education.

Outcomes

Primary Outcomes

Fluid deficit of the elderly

Time Frame: Through study completion, about three years

The elderly in the intervention and control groups; before the training (on the 2nd, 3rd and 4th days of the study), after the training (on the 6th, 7th and 8th days of the research), after the audible stimulus (on the 9th, 10th and 11th days of the research), and 15 days after the audible stimulus monitoring (26, On the 27th and 28th days), the 24-hour amount of urine and the urine concentration was measured and recorded by the nurse.

Total amount of fluids taken by the elderly

Time Frame: Through study completion, about three years

The elderly in the intervention and control groups; before the education (on the 2nd, 3rd and 4th days of the study), after the education (on the 6th, 7th and 8th days of the research), after the audible stimulus (on the 9th, 10th and 11th days of the research), and 15 days after the audible stimulus monitoring (26, On the 27th and 28th days), the total amount of fluid he consumed daily was measured and recorded by the nurse.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Izmir Katip Celebi University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Perihan ÇETİN

Assistant Professor, PhD,

Izmir Katip Celebi University

Study Sites (1)

Loading locations...

Similar Trials