Skip to content

Efficacy Study of Autosuggestion for Quality of Life of Geriatric Patients

Quality of Life and Psycho-Neuro-Endocrine-Immunology Pathway of Geriatric Patients: A Trial of Autosuggestion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01681056
Acronym
ESAQoGe
Enrollment
51
Registered
2012-09-07
Start date
2010-08-31
Completion date
2012-02-29
Last updated
2012-10-03

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

Conditions

Quality of Life for Geriatric Patients.

Keywords

autosuggestion, quality of life, geriatric, serum cortisol, Interferon gamma, interleukin-2, interleukin-6, neuroplasticity

Brief summary

The objective is to analyze the efficacy of autosuggestion for geriatric patients's quality of life and its impact to psycho-neuro-endocrine-immune pathways. The primary outcome is quality of life. The hypothesis of this study is that autosuggestion will increase geriatric patient's quality of life based on its impact to psycho-neuro-endocrine-immune pathways.

Detailed description

Geriatric patients diagnosed with multipathology after getting information and signing informed consent will be included in this trial. Autosuggestion was created by patients according to their preferences, modified by researcher to accomplish autosuggestion principles, recorded in a tape to be heard by walkman daily for 30 days. Intervention and control groups received usual standard medical therapy. Baseline data were collected within one week after admission. Then the subject will be followed up for 30 days. Primary outcome was quality of life measured by COOP chart, analyze using on treatment analysis. Secondary outcomes were serum cortisol, interleukin-2, interleukin-6, IFN-ϒ (Interferon gamma), and N Acetyl Aspartat/ creatine ratio in limbic and paralimbic system by Magnetic Resonance Spectroscopy.

Interventions

BEHAVIORALAutosuggestion for 30 days

Sponsors

Indonesia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Age: ≥ 60 years old with multipathology, inpatients * Not in steroid therapy * Could communicate (Karnofsky score: 40% or Zubrod/WHO score: 3) * Cooperative * Willing to go through all of the research steps.

Exclusion criteria

* Stroke * Multiple Sclerosis * Brain Tumour * Using Pace maker

Design outcomes

Primary

MeasureTime frameDescription
Quality of Life30 daysMeasured by COOP chart

Secondary

MeasureTime frameDescription
Interferon Gamma (pg/mL)30 daysChange from baseline in Interferon Gamma concentration (pg/mL) measured by ELISA method at 08.00-09.00 am.
Interleukin-6 (pg/mL)30 daysChange from baseline in Interleukin-6 concentration(pg/mL) measured by ELISA method at 08.00-09.00 am.
Serum Cortisol (ng/mL)30 daysChange from baseline in Serum Cortisol concentration (ng/mL) measured by Radioimmunoassay method at 08.00-09.00 am.
Interleukin-2 (pg/mL)30 daysChange from baseline in Interleukin-2 concentration (pg/mL) measured by ELISA method at 08.00-09.00 am.
N Acetyl Aspartat/ creatine ratio in limbic and paralimbic system (amygdala, hippocampus, hypothalamus, temporal lobe, accumbens nuclei, prefrontal cortex)30 daysRatio change from baseline by Magnetic Resonance Spectroscopy.

Countries

Indonesia

Outcome results

None listed

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