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Ayurveda regimen on quality of life among elderly population in Ballabhgarh.

An exploratory series of n of 1 responder restricted study of Ayurveda regimen on quality of life among elderly population in Ballabhgarh district of Haryana- A community based study.

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049188
Enrollment
120
Registered
2023-01-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

None listed

Interventions

None listed

Sponsors

Central Council for Research In Ayurveda Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Clinically stable participants who have completed 60 years of age of either gender (Screening assessments for clinically stable participants will be done on the basis of medical history, physical examination, safety laboratory tests (CBC, ESR, LFT, RFT, FBS, PPBS, Lipid profile, VDRL), vital signs, ECG, X-ray) 2. Participants should be in generally good health and those with chronic diseases should be (hypertension, coronary artery disease, etc.) clinically stable with medication and should not affect the day to day activities. 3. Participants fit enough to participate and qualify in the assessment tests while screening. 4. Participants who will voluntarily give consent to participate and comply to the trial interventions strictly for 9 months.

Exclusion criteria

Exclusion criteria: 1. Participants with major systemic illness including liver disease, kidney diseases, and malignancy. 2. Cardiovascular diseases (unstable ischemic heart disease, etc) or uncontrolled blood pressure ( >180/110 mmHg) 3. Uncontrolled Diabetes Mellitus (HbA1C > 8%) 4. Cognitive impairment, neuro-psychiatric diseases which would render the participants unable to participate in the assessment tests. 5. Participant taking participation in any other clinical trial. 6. Any other condition that the Principle investigator thinks may jeopardize the study

Design outcomes

Primary

MeasureTime frame
Change in quality of life in terms of Old peoples Quality Of Life (OPQOL) Questionnaire at five different time lines This is score based and has been used for sample size calculation.Timepoint: 0 months 3 months 5 months 7 months 9 months

Secondary

MeasureTime frame
1. Change in various haematological and biochemical, radiological parameters 2. Changes in physical activity using Barthel index, sleep quality using Pittsburgh Sleep Quality Index and health using swasthya assessment scaleTimepoint: Biomarkers viz. inflammatory, bone health, vascular at 0 3 9 months. questionnaire at 0 3 5 7 9 months dexa at 0 3 9 months

Countries

India

Contacts

Public ContactDr Puneet Misra

AIIMS, New Delhi

drpuneetresearch@gmail.com01126593773

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026