Comparison of follow up of spinal cord injury patients via telehealth vs routine follow up via OPD
Not Applicable
- Conditions
- Health Condition 1: Z718- Other specified counseling
- Registration Number
- CTRI/2021/01/030526
- Lead Sponsor
- Department of Orthopaedics PT BD Sharma PGIMS Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with traumatic Spinal cord injury giving consent for participation in the study
Exclusion Criteria
1.Patients with non traumatic spinal cord injury
2.patients with head injury, medically unstable condition,have cognitive or verbal impairment,have clinically significant medical condition that would compromise participation in the trial
3.patients who dont have access to a phone
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.clinical effectiveness <br/ ><br> a.clinical complications <br/ ><br> b.functional status <br/ ><br>2.psychological health <br/ ><br> a.social participation <br/ ><br> b.quality of life <br/ ><br> c.mental health <br/ ><br>3. patient perspective <br/ ><br> a.patient satisfaction <br/ ><br> b.patient engagement <br/ ><br>4.caregiver perspectiveTimepoint: Following will be assessed at baseline(on discharge) <br/ ><br>At 2 months <br/ ><br>At 6 months <br/ ><br>1.clinical effectiveness <br/ ><br> a.clinical complications <br/ ><br> b.functional status <br/ ><br>2.psychological health <br/ ><br> a.social participation <br/ ><br> b.quality of life <br/ ><br> c.mental health <br/ ><br>3. patient perspective <br/ ><br> a.patient satisfaction <br/ ><br> b.patient engagement <br/ ><br>4.caregiver perspective
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI