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formulation and testing of a mobilization algorithm

Devlopment and testing of a mobilization algorithm in patients recovering from acute heart failure: A multi-method study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047582
Enrollment
50
Registered
2022-11-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: I50- Heart failure

Interventions

Intervention1: mobilisation algorithm: The principal investigator will train the physiotherapists to administer the mobilization algorithm which was developed after 3 rounds of Delphi. Using a validat
developed by American Heart Association for healthcare simulation briefing. The intervention group shall receive standard guideline-directed medical therapy with referral and delivery of EBCR as per

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1) >18 years of either gender 2) NYHA class â?? I-IV 3) Clinically diagnosed with AHF and admitted in the ICU and/or wards of Cardiology, Kasturba Hospital, Manipal 4) Hemodynamically stable patients

Exclusion criteria

Exclusion criteria: 1) Acute myocardial infarction 2) Acute renal injury requiring dialysis 3) Unstable ventricular arrhythmias 4) Neuromuscular impairments affecting mobility 5) Acute exacerbation of COPD

Design outcomes

Primary

MeasureTime frame
6MWTTimepoint: baseline, discharge, 1 month, 3 months and 6 months

Secondary

MeasureTime frame
One minute sit-to-standTimepoint: baseline, discharge, 1 month, 3 months & 6 months;Time-up and go test (TUG)Timepoint: baseline, discharge, 1 month, 3 months and 6 months;Barthel indexTimepoint: baseline, discharge, 1 month, 3 months and 6 months;Kansas city cardiomyopathy questionnaire- 12 (KCCQ-12)Timepoint: baseline, discharge, 1 month, 3 months and 6 months;Adverse eventsTimepoint: baseline, discharge, 1 month, 3 months and 6 months;Event free daysTimepoint: baseline, discharge, 1 month, 3 months and 6 months;Exercise adherenceTimepoint: baseline, discharge, 1 month, 3 months and 6 months;MACETimepoint: baseline, discharge, 1 month, 3 months & 6 months;Feasibility assessment using the Donabedian modelTimepoint: during the study & at discharge;Acceptability of intervention assessment using the Theoretical Acceptability FrameworkTimepoint: during the study & at discharge

Countries

India

Contacts

Public ContactAkhila Satyamurthy

MCHP, Manipal, MAHE

abrahambabu@gmail.com

Outcome results

None listed

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