ClinicalTrials.Veeva

Menu

The Effect of Audible Alarm on the Fluid Consumption of the Elderly

I

Izmir Katip Celebi University

Status

Completed

Conditions

The Elderly

Treatments

Behavioral: Intervention group
Behavioral: Control group

Study type

Interventional

Funder types

Other

Identifiers

NCT04242745
17-7.1/36 27.07.2017;

Details and patient eligibility

About

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.

Enrollment

100 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Intervention group
Experimental group
Description:
Procedure/Surgery:The intervention group was given education and a wristwatch which gave an audible alarm to remind them to drink liquid.
Treatment:
Behavioral: Intervention group
Behavioral: Control group
Control group
No Intervention group
Description:
The control group was given only education.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems