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Robotics as a Useful Tool to Improve the Hydration of the Elderly

Not Applicable
Completed
Conditions
Daily Fluid Intake
Dehydration
Urinary Infections
Interventions
Device: humanoid robot
Other: Usual care
Registration Number
NCT06520033
Lead Sponsor
Universitat de Lleida
Brief Summary

The aim of this clinical trial is to evaluate the effectiveness of a hydration educational program executed through a robot in comparison with the usual hydration program in terms of fluid intake and general health status of the residents. The main question to be answered is whether the use of robotics through a humanoid robot increases the hydration of institutionalized older people.

Participants:

* The intervention group will receive a hydration plan executed by the robot and the control group will receive the center\'s usual hydration plan.

* Healthcare personnel will receive reminders from the robot to record fluid intake through it. In the control group, health personnel will perform the fluid intake record in paper format and at the end of the shift, as usual.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
57
Inclusion Criteria
  • Age equal to or greater than 65 years.

No exclusion criteria have been established.

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention grouphumanoid robotThe intervention group will receive a hydration plan executed by a humanoid robot. Healthcare personnel will receive reminders from the robot to record fluid intake through it.
Control group withUsual careThe control group will receive the center's usual hydration plan. The health personnel will make the fluid intake record in paper format and at the end of the shift, as usual.
Primary Outcome Measures
NameTimeMethod
Blood Urea Nitrogen8 weeks

BUN = Urea/2.1428. Dehydration \> 20mg/dl

Number of urinary infections8 weeks

Obtained through a urine sample and evaluated with the Combur-Test.

Daily fluid intakeFrom enrollment to the end of intervention at 8 weeks

Amount in milliliters (ml)

Urine color8 weeks

Urine color chart (Armstrong, 2000). Values = 1 - 8. Dehydration: scores \>= 4

Serum osmolarity8 weeks

Serum osmolarity: \[1,86\*(Na+K)+1,15\*Glucose+urea+14)\]. Dehydration \> 300mOsm/kg

Secondary Outcome Measures
NameTimeMethod
Risk of falls8 weeks

Downton scale. Values = 0 - 11. Risk of falls: scores \> 2

Pharmacological treatment8 weeks

Number of medicines taken by the participant per day and type of medicine.

Hospital admissions8 weeks

Number of hospital admissions

Illnesses8 weeks

Diseases that the participant currently presents

Dry Skin8 weeks

Skin turgor: if skin remains elevated after being pulled up and released

Efficacy and safety of swallowing8 weeks

Volume-Viscosity swallow test (V-VST): identify clinical signs of impaired efficacy (labial seal, oral and pharyngeal residue, and piecemeal deglutition) and impaired safety of swallow (voice changes, cough and decrease in oxygen saturation ≥3%). It starts with nectar viscosity and increasing bolus volume, then liquid and finally pudding viscosity

Nutritional status8 weeks

Assessed through the Mini Nutritional Assessment (MNA). Values = 0 - 30. Malnutrition: scores \< 17

Risk of pressure ulcers8 weeks

Braden Scale. Values = 6 - 23. Risk of pressure ulcers: scores \< 19

Functional status8 weeks

Barthel index. Values = 0 - 100. Functional impairment: scores \< 90

Cognitive status8 weeks

Global Deterioration Scale (GDS). Values = 1 - 7. Dementia: scores \>= 3

Trial Locations

Locations (1)

Residència i Centre de Dia per a Gent Gran Balàfia II

🇪🇸

Lleida, Spain

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