The Effect of Teleconsultation, on the Reversibility of Frailty in Geriatric Patients Post Hospitalization

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60+
SponsorIndonesia University

About this trial

The goal of this clinical trial is to learn if a structured tele-consultation program, delivered 3 times over 12 weeks, can improve (reverse) frailty in geriatric patients recently discharged from the hospital. The main questions it aims to answer are:

* Does structured tele-consultation covering physical exercise, nutrition, and home care education change health behavior in older adults after hospital discharge? * Does this change in health behavior lead to improvement in frailty, as measured by Clinical Frailty Scale (CFS) score? * Does this change in health behavior lead to improvement in frailty, as measured by decreased interleukin-6 (IL-6) and myostatin levels and increased albumin levels? * Does this change in health behavior lead to improvement in frailty, as measured by increased hand grip strength?

Researchers will compare participants receiving structured tele-consultation (delivered 3 times over 12 weeks) to participants receiving usual care to see if tele-consultation leads to greater improvement in health behavior and frailty status.

Participants will:

* Undergo baseline assessment of CFS score, hand grip strength, and blood sampling for IL-6, albumin, and myostatin shortly after hospital discharge * Be randomly assigned to receive either structured tele-consultation (3 sessions over 12 weeks, covering physical exercise, nutrition, and home care education) or usual care * Undergo repeat assessment of health behavior, CFS score, hand grip strength, and the same blood markers at the end of the 12-week period

Eligibility criteria

Qualifiers

Age 60 years or older

Approved for hospital discharge

Diagnosed with pre-frailty or frailty

Access to a mobile phone, tablet, or laptop

Disqualifiers

Unwilling to participate in the study

Depression, as indicated by a Geriatric Depression Scale (GDS) score ≥10, assessed at the time of discharge

Moderate to severe cognitive impairment, as indicated by a Montreal Cognitive Assessment-Indonesian version (MoCA-INA) score <26, assessed at the time of discharge

Severe frailty, as indicated by a Clinical Frailty Scale (CFS) score >8

Trial design

Treatments tested in this trial

  • structured teleconsultation and face to face consultation
  • face to face consultation

Treatment groups

116 Participants
are divided into 2 treatment groups

Sponsors and collaborators