NCT06846177 Graded Activity Training and Task- Oriented Training on Post-Stroke Fatigue
| NCT ID | NCT06846177 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Riphah International University |
| Condition | Post-Stroke Fatigue |
| Study Type | INTERVENTIONAL |
| Enrollment | 20 participants |
| Start Date | 2025-03-01 |
| Primary Completion | 2026-03-20 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 20 participants in total. It began in 2025-03-01 with a primary completion date of 2026-03-20.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of this randomized controlled trial is to determine the effects of Graded Activity Training and Task Oriented Training on Fatigue in Post-Stroke Patients. Until now there is very limited work found on fatigue so this will increase quality of life in stroke patients and potentially reduce burden on healthcare system.
Eligibility Criteria
Inclusion Criteria: * Both male and female of age 40 to 60 years. * Patient with both ischemic or hemorrhagic stroke. * Patient with both right and left hemiplegia. * Checklist Individual (CIS-F) fatigue score of 40 or more. * Patients who had sustained a stroke more than 4 months before recruitment. * Patients who can independently walk for 10 meters (about 33 feets) Exclusion Criteria: * Patients with severe comorbid health conditions (such as cardiac diseases, pulmonary diseases like COPD, Orthopedic Conditions Arthritis, joint replacements). * Patients with uncontrolled diabetes, hypertension, Depression and Anxiety. * Patients who are not willing to participate. * Patient with any medications that can affect their ability to engage in physical training program like Antidepressants, Beta-Blockers, corticosteroids etc. * Pregnant women.
Contact & Investigator
Dr.Aroosa Tariq, MS-NMPT
PRINCIPAL INVESTIGATOR
Riphah International University
Frequently Asked Questions
Who can join the NCT06846177 clinical trial?
This trial is open to participants of all sexes, aged 40 Years or older, up to 60 Years, studying Post-Stroke Fatigue. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06846177 currently recruiting?
Yes, NCT06846177 is actively recruiting participants. Contact the research team at aroosa.tariq@riphah.edu.pk for enrollment information.
Where is the NCT06846177 trial being conducted?
This trial is being conducted at Mansehra, Pakistan.
Who is sponsoring the NCT06846177 clinical trial?
NCT06846177 is sponsored by Riphah International University. The principal investigator is Dr.Aroosa Tariq, MS-NMPT at Riphah International University. The trial plans to enroll 20 participants.
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