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Smart App for Faster Healing after hip surgery in elderly population

EVALUATION OF EFFECTIVENESS OF MOBILE BASED APPLICATION VERSUS CONVENTIONAL REHABILITATION FOR THE RADIOLOGICAL AND FUNCTIONAL OUTCOME OF POST SURGICAL MANAGEMENT OF HIP FRACTURES IN GERIATRIC PATIENTS - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080721
Enrollment
30
Registered
2025-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: S720- Fracture of head and neck of femur

Interventions

Intervention1: Mobile Application ORTHOFLEX HIP : Patients undergoing hip surgeries will use the mobile application "ORTHOFLEX HIP" as part of their post-operative rehabilitation protocol. The app p

Sponsors

Sajith S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Confirmed hip Surgery: Participants must have undergone surgical procedure for hip ( such as hemiarthroplasty, THR, proximal femur nailing) 2. Age Range: Participants aged more than 50 years and older are eligible for inclusion. 3. Time Since Surgery: Participants should be within a specified timeframe post-surgery, typically within the initial stages of rehabilitation (e.g., within the first 12 weeks post-surgery). 4. Functional Status: Participants should have a baseline level of functional mobility and independence, as determined by the treating physician or healthcare provider. 5. Ability to Understand and Follow Instructions: Participants must possess the cognitive ability to understand and follow the instructions provided as part of the rehabilitation program. 6. Consent: Participants must provide informed consent to participate in the rehabilitation program and any associated

Exclusion criteria

Exclusion criteria: 1) Previous hip Surgery: Participants who have undergone previous hip surgery on the same limb are excluded from participation. 2) Severe Comorbidities: Participants with severe comorbidities or medical conditions that may interfere with rehabilitation or increase the risk of complications are excluded. 3) Uncontrolled Medical Conditions: Participants with uncontrolled medical conditions, such as uncontrolled hypertension or diabetes, that may pose a risk during rehabilitation are excluded. 4) History of Adverse Reactions to Rehabilitation Interventions: Participants with a history of adverse reactions or complications related to previous rehabilitation interventions are excluded.

Design outcomes

Primary

MeasureTime frame
Enhanced functional recovery, including improvements in hip function, range of motion, strength, and mobility, as measured by validated clinical scales over the study period.Timepoint: At 12 weeks post surgery

Secondary

MeasureTime frame
Improved rehabilitation adherence rates assessed through engagement metrics in the mobile application. Increased patient satisfaction evaluated via standardized satisfaction surveys. Reduction in healthcare utilization, including fewer in-person visits and lower medical costs.Timepoint: 3 months

Countries

India

Contacts

Public ContactDr Benjamin vinodh J

Saveetha medical college and hospital

Benjaminvinodh91@gmail.com9445711147

Outcome results

None listed

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