An interventional study of Structured Patient-Centered Educational Program. in Hip Fractures, sponsored by Assiut University. Recruiting at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2026-09-09.
Sponsored by Assiut University · Not applicable, Interventional, and Treatment
Among 12 studies in Hip Fractures by Assiut University — 7 open to participants now, 7 under way, 3 of them phase 3. Hip Fractures · Assiut University.
Among the 12 studies in Hip Fractures by Assiut University, this one is one of 2 that started in 2026, is one of 3 with no phase, and was the 10th registered.
842 studies on the registry are indexed under Hip Fractures; 165 are open to participants now.
Browse Hip Fractures studies →7 of the 12 studies in Hip Fractures by Assiut University are open now, in 1 country. Recruiting first, the newest first:
Assiut University · Sites in Egypt
Assiut University
Assiut University
Assiut University
Assiut University
By country, each count listing its studies:
Of the 104 Hip Fractures studies recruiting now, 82 (79%) set no upper age limit and 6 (6%) stop at 75 or younger; 12 take children under 18; 9 take healthy volunteers.
This study: all sexes · healthy volunteers too.
The full table on the hub →This tab as a report to print or save as PDF → With an account.
12 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 2 2 · Phase 3 3
First in 2010; this study’s year is marked. 2 started in 2026.
This study's planned enrollment of 100 is above the median of 86 across 533 interventional studies indexed under Hip Fractures.
Median enrollment 59 across the 6 interventional studies, 118 across the 6 observational. Of the 3 that completed or were terminated, 0 (0%) have results posted.
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Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.
Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
2 of the studies in Hip Fractures by Assiut University that are under way reach primary completion within a year, 1 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT07810556Phase 3Assiut UniversityIntrathecal Dexmedetomidine and Postoperative Delirium in Elderly Hip Fracture Surgery | 2027-10 |
| NCT07739225Assiut UniversityPatient-Centered Education After Hip Fracture Surgery | 2027-02-05 |
Among the 12 studies in Hip Fractures by Assiut University, from their registry updates:
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This randomized controlled trial aims to evaluate the effect of a structured patient-centered educational program on postoperative outcomes among patients undergoing hip fracture surgery. Participants will be randomly assigned to either an intervention group receiving the educational program in addition to routine care or a control group receiving routine care only. The study will assess whether the educational program improves postoperative recovery, functional independence, and pain outcomes following hip fracture surgery.
Hip fracture is a major cause of disability, functional decline, and increased healthcare utilization among older adults. This study is a parallel-group randomized controlled trial conducted at the Orthopedic Department and Orthopedic Outpatient Clinics of Qena University Hospital. Participants will be randomly allocated in a 1:1 ratio to either an intervention group receiving a structured patient-centered educational program in addition to routine postoperative care or a control group receiving routine postoperative care alone. Randomization will be performed using computer-generated random numbers with allocation concealment using sealed opaque envelopes, and outcome assessment will be conducted by a blinded assessor. The educational program includes education on postoperative care, pain management, safe mobility, rehabilitation exercises, activities of daily living, prevention of postoperative complications, and discharge planning, supported by an illustrated educational booklet. Participants will be followed from the preoperative assessment through hospital discharge and scheduled postoperative follow-up visits.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Participants in this group will receive a structured patient-centered educational program in addition to routine postoperative care.
Behavioral: Structured Patient-Centered Educational Program.
Participants in this group will receive routine postoperative care only.
A structured educational program focusing on postoperative care, pain management, rehabilitation exercises, safe mobility, prevention of complications, and activities of daily living, supported by an illustrated educational booklet.
Functional Independence Measure (FIM) Total Score.
The Functional Independence Measure (FIM) will be used to assess functional independence following hip fracture surgery. The FIM consists of 18 items with a total score ranging from 18 to 126. Higher scores indicate greater functional independence and better postoperative functional outcomes.
Time frame: Baseline (preoperative), at hospital discharge (assessed up to 4 days after surgery), 1 month after surgery, and 3 months after surgery.
Visual Analog Scale (VAS) Pain Score.
Pain intensity will be assessed using the Visual Analog Scale (VAS). The VAS ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity.
Time frame: Baseline (preoperative), at hospital discharge (assessed up to 4 days after surgery), 1 month after surgery, and 3 months after surgery.
Plan to share: No — IPD will not be shared with other researchers. Participant data will remain confidential and will only be used for the purposes of this study in accordance with ethical research principles and institutional regulations.
No publications or documents are linked to this record.
Started Sep 2026 (actual). Primary completion is estimated for Feb 2027, 5 months after the start.
Of 221 non-industry interventional studies with no phase under Hip Fractures, half reached primary completion within 27 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 55. This study's planned 5 months is below that.
Counting every sponsor, half of 237 studies reached it within 29 months; a quarter within 10 and three quarters within 57.
How these figures are worked out, and which studies are left out of them.
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