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Effectiveness of a Telegeriatric Intervention in Older Adults During the Covid-19 Contingency

Effectiveness of a Telegeriatric Intervention in Older Adults During the Covid-19 Contingency

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04747132
Enrollment
110
Registered
2021-02-10
Start date
2020-07-20
Completion date
2020-11-16
Last updated
2021-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Effectiveness

Keywords

Aged, Internet-Based Intervention, COVID-19

Brief summary

The purpose of this studdy is to assess the effectiveness of a telegeriatric intervention

Detailed description

The patients were recruited from a cohort study in which the participants had previously signed an informed consent in which they allowed contact to participate in new studies, participants who met the inclusion criteria in the original database were recruited and signed an electronic informed consent of the new study. A comprehensive geriatric assessment was generated to assess whether they were candidates even due to changes in health status that could change over time since their last assessment, they were recruited until the expected sample size was obtained, and they were randomized, blinding the participants to belong to the intervention group (individualized care: geriatrics, psychology, physical activity and nutrition) or the control group (orientation in standardized health issues through audiovisual educational material)

Interventions

OTHERTelegeriatric intervention

Individualized, comprehensive and specialized counseling for older adults through the Internet

Sponsors

Universidad Iberoamericana A.C., Mexico
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults 60 years and over * Who agree to participate in the study.

Exclusion criteria

* Older adults who are in a systematic exercise program or directed food restriction programs * Physical, sensory or cognitive disabilities that prevent exercise, includes Mini Mental State Examination less than 20 points of the total score * Any condition acute or chronic health conditions that clinical staff judge as an impediment to the exercise program or remote monitoring * Recent major or limb surgery * Orthopedic conditions that would impede the exercise program * Any problem swallowing * Previous mental disorders such as disorder and schizophrenia * Not having personal access to the WhatsApp application via video call.

Design outcomes

Primary

MeasureTime frameDescription
Visual analog scale of the European quality of life questionnaireChange from baseline to week 12The visual analog scale of the European quality of life questionnaire, adapted and validated to Spanish, Mexico (EQ5D-VAS) will be used. Which consists of a visual analog scale, its total score ranges from 0 to 100 points, the higher the score, the better the quality of life, it will be considered as a continuous quantitative variable. (Juárez-Cedillo T et al., 2015) Change from baseline to week 12
Physical performance.Change from baseline to week 12It will be evaluated through the short physical performance test (SPPB), which is a test that includes three dimensions: strength. March and balance, your score ranges from 0 to 12 points, the higher the score the better the physical performance, it will be considered as a continuous quantitative variable. (Guralnik JM et al., 1989) Change from baseline to week 12
Depressive symptomsChange from baseline to week 12It will be evaluated using the CESD scale 7 items validated into Spanish in Mexico. His score ranges from 0 to 21 points, the higher the score, the greater the depressive symptoms. The total score will be considered as a continuous quantitative variable. (Salinas-Rodríguez A et al., 2014) Change from baseline to week 12
Symptoms of anxiety.Change from baseline to week 12It will be evaluated through the geriatric anxiety inventory, which is validated in Spanish, consists of 20 dichotomous items, its total score ranges from 0 to 20, the higher the score, the greater the anxiety symptoms. It will be considered as a continuous quantitative variable. (Márquez-González M et al., 2012) Change from baseline to week 12
Body compositionChange from baseline to week 12It will be evaluated by using the OMROM HBF-514C® 50 Hz portable electrical bioimpedance bascule Change from baseline to week 12
Anthropometric measuresChange from baseline to week 12It will be evaluated by using the SECA anthropometric tape Change from baseline to week 12
Dietary intakeChange from baseline to week 12It will be evaluated by using the ASA24 software for 24-hour reminder collection by multiple steps. Change from baseline to week 12

Countries

Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026