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Understanding Stroke Recovery: What Improves During Hospital Rehabilitation?

Prospective Observational Study on Quality of Life, Disability, Upper Limb Function, and Gait Parameters in Stroke Patients Following Inpatient Rehabilitation - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/12/098560
Enrollment
122
Registered
2025-12-05
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Health Condition 1: I639- Cerebral infarction, unspecified

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

All India Institute of Medical Sciences (AIIMS), Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged more than 18 years with recent stoke less than 1 year old ischemic or hemorrhagic stroke. Medically stable and admitted for inpatient rehabilitation. Able to provide informed consent and participate in assessments.

Exclusion criteria

Exclusion criteria: Pre-stroke mRS more than 4 Non-ambulatory status prior to stroke.

Design outcomes

Primary

MeasureTime frame
Change in health-related quality of life (HRQoL) measured by the EQ-5D-5L index from admission (baseline) to 24 weeks post-discharge.Timepoint: Change in health-related quality of life (HRQoL) measured by the EQ-5D-5L index from admission (baseline) to 24 weeks post-discharge.6, 12, and 24 weeks

Secondary

MeasureTime frame
1. To evaluate the change in functional disability using the Modified Rankin Scale (mRS) 2. To evaluate the change in functional independence level by Barthel Index (BI). 3. To measure upper limb motor recovery using the Fugl-Meyer Assessment (Upper Limb subscore). 4. To analyze gait improvements using spatiotemporal analysis and the Timed Up and Go (TUG) test. 5. To assess psychological status using the Hospital Anxiety and Depression Scale (HADS). Timepoint: 6, 12, and 24 weeks

Countries

India

Contacts

Public ContactRavi Gaur

All India Institute of Medical Sciences (AIIMS), Jodhpur

ravisms80@gmail.com7907102168

Outcome results

None listed

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