Tibial FractureNCT07810478
Criteria-Based Rehabilitation After Tibial Fracture Fixation: A Randomized Controlled Trial
A study testing Criteria-Based Progressive Loading and Functional Rehabilitation Program in people with Tibial Fracture, run by Al-Azhar University at 1 site in Palestinian Territories.
Trial summary
This randomized controlled trial will evaluate the effectiveness of a criteria-based progressive loading and functional rehabilitation program compared with usual physiotherapy in adults following surgical fixation of traumatic tibial fractures in Gaza. Read more about this study
- Who is it for?
- Ages 18 to 60 yearsHealthy volunteers can take part
- Conditions the study is for
- Tibial Fracture
- What is being tested?
- Criteria-Based Progressive Loading and Functional Rehabilitation Program
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 1 sitePalestinian Territories
- Study dates
- 18 Sep 2026to 1 Jul 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Age ≥18 years.
- Traumatic unilateral tibial fracture involving the proximal tibia/tibial plateau, tibial shaft, or distal tibia.
- Treated with surgical fixation.
- Recruitment 2-8 weeks after the index fixation surgery.
- Medically and surgically stable and cleared by the treating team to participate in physiotherapy.
- Documented postoperative weight-bearing status/instructions from the treating orthopedic team.
Show all 9Show fewer
- Able to participate in the study rehabilitation and complete the planned functional assessments when permitted by weight-bearing status.
- Able to understand study instructions and provide written informed consent.
- Open fractures are eligible provided the wound is clinically stable, there is no active uncontrolled infection preventing rehabilitation, and rehabilitation has been authorized by the treating surgical team.
Who cannot join
- Pathological fracture.
- Unstable fixation, fixation failure, or any orthopedic/medical contraindication to progressive rehabilitation.
- Active or uncontrolled infection requiring restriction or interruption of rehabilitation.
- Lower-limb amputation affecting functional assessment.
- Spinal cord injury or severe traumatic brain injury affecting mobility or ability to participate.
- Pre-existing neurological disorder substantially affecting gait or lower-limb function.
Show all 9Show fewer
- Major concomitant injury to either lower limb that substantially limits walking or participation in the rehabilitation protocol.
- Severe cognitive impairment preventing understanding of instructions, valid outcome assessment, or informed consent.
- Any medical condition considered by the treating physician to make participation in the rehabilitation program unsafe.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Palestinian Territories1 site, 1 recruiting
- Recruiting
Mohammed Matar
Gaza, Gaza Strip
Naser medical complex Lecturers, master, 0097097075397, matar772015@gmail.com
About this study
Official title: Effectiveness of a Criteria-Based Progressive Loading and Functional Rehabilitation Program Compared With Usual Physiotherapy Following Surgical Fixation of Traumatic Tibial Fractures: A Randomized Controlled Trial
This randomized controlled trial will evaluate the effectiveness of a criteria-based progressive loading and functional rehabilitation program compared with usual physiotherapy in adults following surgical fixation of traumatic tibial fractures in Gaza. Participants will be randomly allocated to either a structured 6-8-week rehabilitation program, in which progression is guided by predefined clinical and functional criteria while respecting orthopedic weight-bearing restrictions, or to usual physiotherapy. The primary outcome will be lower-limb function measured using the Lower Extremity Functional Scale (LEFS). Secondary outcomes will include functional mobility, walking endurance, pain, knee and ankle range of motion, functional ambulation, walking-aid dependence, and adverse events. Outcomes will be assessed at baseline, post-intervention, and follow-up. The study aims to determine whether a standardized criteria-based rehabilitation approach can improve functional recovery following traumatic tibial fracture fixation.
Read the detailed description
### Detailed Intervention Prescription
Participants allocated to the intervention group will receive a structured criteria-based progressive loading and functional rehabilitation program for approximately 6-8 weeks, consisting of 2-3 supervised physiotherapy sessions per week in addition to an individualized home exercise program. Each supervised session will last approximately 45-60 minutes and will include an individualized combination of joint mobility, muscle strengthening, balance, gait, and functional training according to the participant's clinical status and stage of recovery.
The fundamental principle of the intervention is that progression will be determined by predefined clinical and functional criteria rather than postoperative time alone. All weight-bearing and loading activities will strictly follow the restrictions prescribed by the treating orthopedic or surgical team. The physiotherapist will not independently advance a participant beyond the medically permitted weight-bearing level.
Phase 1: Protection and Early Mobility
During the initial phase, rehabilitation will focus on protecting the surgical site, controlling symptoms, maintaining joint mobility, minimizing muscle weakness, and achieving safe basic mobility. Treatment will include patient education, appropriate positioning, pain and edema management, active or active-assisted knee and ankle range-of-motion exercises as clinically permitted, quadriceps activation, hamstring and gluteal exercises, ankle exercises, and straight-leg raising when appropriate. Muscle activation and mobility exercises will generally be performed for 2-3 sets of 10-15 repetitions according to the participant's tolerance.
Functional rehabilitation during this phase will include bed mobility, transfer training, sit-to-stand practice when appropriate, and instruction in the safe use of crutches or a walker according to the prescribed weight-bearing status. Participants will also receive an individualized home exercise program focusing primarily on mobility and muscle activation.
Progression from this phase will not occur simply because a predetermined number of postoperative weeks has elapsed. Progression will be considered when the participant demonstrates satisfactory wound and soft-tissue status, controlled pain and swelling, improving knee and ankle mobility, safe transfers, appropriate performance of the prescribed exercises, and adequate neuromuscular control.
Phase 2: Initial Loading and Gait Rehabilitation
This phase will begin once increased loading or weight-bearing has been medically permitted by the orthopedic or surgical team. Treatment will focus on gradually introducing the permitted load to the affected limb and restoring safe functional mobility.
Interventions will include controlled weight-shifting activities, weight-bearing practice within the prescribed limits, gait retraining using the appropriate walking aid, progressive lower-limb strengthening, sit-to-stand training, supported balance exercises, continued knee and ankle mobility exercises, and progressive walking practice. Strengthening exercises will generally be performed for 2-3 sets of approximately 8-15 repetitions, with resistance adjusted according to the participant's clinical status and ability to perform the movement with appropriate control.
Gait training will emphasize safe loading of the affected limb within the prescribed restriction, appropriate step pattern, correct use of the walking aid, balance, and progressive improvement in walking quality. Walking duration and distance will be increased gradually according to tolerance.
Progression will be considered when the participant can tolerate the currently prescribed loading level without clinically significant worsening of pain, swelling, or other symptoms; demonstrate controlled weight transfer; perform functional activities with satisfactory movement control; and walk safely using the prescribed assistive device. Advancement to a higher weight-bearing level will occur only when permitted by the treating orthopedic team.
Phase 3: Progressive Functional Loading
As greater weight-bearing is medically permitted, rehabilitation will progressively emphasize functional loading, lower-limb strength, balance, gait quality, and independence. Treatment will include progressive closed-chain exercises, functional strengthening, repeated sit-to-stand practice, step-up and step-down activities, balance and proprioceptive exercises, progressive walking, and gait-quality training.
Exercises will generally be prescribed for approximately 2-4 sets of 8-15 repetitions depending on the exercise, participant tolerance, and functional goal. The difficulty of exercises will be progressively increased by modifying resistance, repetitions, movement complexity, balance demands, walking distance, or the amount of upper-limb support rather than progressing according to time alone.
Reliance on crutches, a walker, or other upper-limb support will be reduced gradually when clinically appropriate and when consistent with the prescribed weight-bearing status. The participant must demonstrate adequate balance and safe gait before progressing to a less supportive walking aid.
Progression to advanced functional rehabilitation will require satisfactory tolerance of the current loading level, controlled symptoms, adequate movement quality, improving functional mobility and balance, safe ambulation, and medical permission for further loading.
Phase 4: Advanced Functional Rehabilitation
Once full weight-bearing is medically permitted, rehabilitation will focus on restoring independent mobility and preparing the participant for community, daily living, and occupational activities. Treatment will include independent gait training, stair negotiation, uneven-surface walking, functional squatting, advanced balance and proprioceptive exercises, progressive lower-limb strengthening, walking endurance training, community mobility activities, and activities of daily living.
Where relevant, rehabilitation will also include work-, household-, or activity-specific tasks based on the participant's individual functional requirements. Walking duration and distance will be progressively increased, and the participant will be encouraged to achieve safe mobility with the least restrictive walking aid or without an assistive device when appropriate.
Throughout all phases, the physiotherapist will assess pain, swelling, range of motion, functional performance, gait safety, exercise tolerance, and any adverse clinical response. Exercise intensity or loading will be reduced or temporarily withheld if the participant develops clinically significant worsening of pain or swelling, wound problems, loss of functional performance, or other signs requiring medical reassessment. Suspected fixation-related complications, wound complications, or other significant adverse events will be referred to the treating medical or surgical team.
The home exercise program will be individualized according to the participant's current rehabilitation phase. Mobility and muscle-activation exercises may be performed daily, while strengthening, balance, gait, and functional activities will be prescribed according to clinical tolerance and safety. Adherence to the home program and supervised physiotherapy sessions will be documented.
The main distinction between this intervention and usual physiotherapy is therefore not the individual exercises themselves. Participants receiving usual physiotherapy may also receive range-of-motion exercises, strengthening, gait training, balance exercises, walking-aid training, and functional exercises. In the intervention group, however, rehabilitation will follow a standardized criteria-based pathway in which advancement, regression, and functional progression are determined by predefined clinical and functional milestones while remaining within the weight-bearing restrictions established by the orthopedic team.
- Conditions
- Tibial Fracture
- Being tested
- Criteria-Based Progressive Loading and Functional Rehabilitation Program
- Keywords
- tibial fractures, Criteria-based rehabilitation, Progressive loading, Weight-bearing; Functional rehabilitation, Functional recovery
- Medical subject headings
- Tibial Fractures
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Criteria-Based Progressive Loading and Functional Rehabilitation ProgramOther
Participants will receive a structured Criteria-Based Progressive Loading and Functional Rehabilitation Program for 12 weeks, consisting of 2-3 supervised physiotherapy sessions per week plus an individualized home exercise program. Rehabilitation will progress through four phases: protection and early mobility; initial loading and gait rehabilitation; progressive functional loading; and advanced functional rehabilitation. Treatment will include pain and edema management, knee and ankle range-of-motion exercises, progressive lower-limb strengthening, weight-shifting and permitted weight-bearing practice, gait training, balance and proprioceptive exercises, sit-to-stand and step training, progressive walking, endurance training, and functional mobility activities. Progression will be based on predefined clinical and functional criteria rather than time alone and will remain within orthopedic weight-bearing restrictions. Participants will be followed for an additional 3 months after comp
| Study group | Role | What they receive |
|---|---|---|
| Criteria-Based Progressive Loading and Functional Rehabilitation | Experimental | Participants assigned to the experimental arm will receive a structured criteria-based progressive loading and functional rehabilitation program for approximately 6-8 weeks, with 2-3 supervised physiotherapy sessions per week in addition to an individualized home exercise program.
The program will progress through four rehabilitation phases according to predefined clinical and functional criteria rather than postoperative time alone. Phase 1 will focus on protection and early mobility and may include pain and edema management, positioning, knee and ankle range-of-motion exercises, quadriceps activation, hamstring and gluteal exercises, ankle exercises, bed mobility, transfer training, and safe use of walking aids. Phase 2 will introduce medically permitted loading through controlled weight shifting, weight-bearing practice, gait retraining, progressive strengthening, sit-to-stand training, supported balance exercises, and progressive walking. Phase 3 will emphasize progressive functi Receives: Other: Criteria-Based Progressive Loading and Functional Rehabilitation Program |
| Usual Physiotherapy | Active comparator | Participants assigned to the control arm will receive the usual physiotherapy rehabilitation routinely provided at the participating rehabilitation centers following surgical fixation of traumatic tibial fractures.
Usual physiotherapy may include pain and edema management, knee and ankle range-of-motion exercises, muscle strengthening, gait training, balance exercises, walking-aid training, functional exercises, progressive walking, and home exercise advice according to routine clinical practice and the individual needs of the participant.
Weight-bearing and loading will follow the instructions provided by the treating orthopedic or surgical team. Unlike the experimental arm, progression of rehabilitation will not be guided by the standardized study-specific criteria-based progression algorithm. The number and duration of physiotherapy sessions and the principal interventions received will be documented throughout the study. Receives: Other: Criteria-Based Progressive Loading and Functional Rehabilitation Program |
What is being measured
The primary outcome is the main question the study is designed to answer.
Lower Extremity Functional Scale
The LEFS will be used to assess lower-limb functional status and the participant's difficulty performing everyday activities. The scale consists of 20 items, each scored from 0 to 4, producing a total score ranging from 0 to 80. Higher scores indicate better lower-extremity function. The primary endpoint will be the between-group difference in change in LEFS from baseline to completion of the intervention.
Measured: pre, 12 weeks post and 3 months follow up
Timed Up and Go Test (TUG)
Functional mobility will be assessed using the TUG. Participants will stand from a chair, walk 3 meters, turn, walk back to the chair, and sit down. The total time required to complete the task will be recorded in seconds, with a shorter time indicating better functional mobility. The test will only be performed when medically appropriate according to the participant's weight-bearing status
Measured: pre, 12 weeks post and 3 months follow up
Numeric Pain Rating Scale (NPRS)
Pain intensity will be measured using an 11-point numeric rating scale from 0 to 10, where 0 represents no pain and 10 represents the worst imaginable pain. Lower scores indicate less pain. Pain at rest and/or during functional activity will be documented according to the study assessment protocol
Measured: pre, 12 weeks post and 3 months follow up
Functional Ambulation Category
The FAC will be used to classify the participant's level of functional walking independence and the amount of physical assistance required during ambulation. It is an ordinal scale ranging from 0 to 5, where 0 indicates inability to walk or the need for assistance from two or more people and 5 indicates independent ambulation. Higher scores indicate greater walking independence
Measured: pre, 12 weeks post and 3 months follow up
Secondary outcomes (2)
ROM
ROM will be measured
Measured: pre, 12 weeks post and 3 months follow up
Walking-Aid Dependence
The type of assistive device required for walking will be recorded at each assessment. Categories will include walker, two crutches, one crutch, cane, or no walking aid. Changes toward a less supportive device or independent walking will be used as a clinically meaningful indicator of functional recovery
Measured: pre, 12 weeks post and 3 months follow up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Sep 2026
- Study start18 Sep 2026
- Primary completion1 Jun 2027 (estimated)
- Study completion1 Jul 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Tibial FractureStudies of the same condition, open and under way.
- More trials run by Al-Azhar UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Al-Azhar University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mosab ALdabbas, Al-Azhar University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07810478
- Sponsor's protocol ID
- Al-Azhar
- Status last verified
- Sep 2026
- First submitted
- 3 Sep 2026
- Last updated
- 21 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Binkley JM, Stratford PW, Lott SA, Riddle DL. The Lower Extremity Functional Scale (LEFS): scale development, measurement properties, and clinical application. North American Orthopaedic Rehabilitation Research Network. Phys Ther. 1999 Apr;79(4):371-83.
PubMed 10201543
Study at a glance
From the registry record, last updated by the sponsor on 21 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of a Criteria-Based Progressive Loading and Functional Rehabilitation Program Compared With Usual Physiotherapy Following Surgical Fixation of Traumatic Tibial Fractures: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT07810478
- Acronym / sponsor ID
- Al-Azhar
- Conditions
- Tibial Fracture
- Keywords
- tibial fractures, Criteria-based rehabilitation, Progressive loading, Weight-bearing; Functional rehabilitation, Functional recovery
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- Al-Azhar UniversityUniversity, hospital or other
- Study start
- 18 Sep 2026 (actual)
- Primary completion
- 1 Jun 2027 (estimated)
- Study completion
- 1 Jul 2027 (estimated)
- First posted
- 9 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This randomized controlled trial will evaluate the effectiveness of a criteria-based progressive loading and functional rehabilitation program compared with usual physiotherapy in adults following surgical fixation of traumatic tibial fractures in Gaza. Participants will be randomly allocated to either a structured 6-8-week rehabilitation program, in which progression is guided by predefined clinical and functional criteria while respecting orthopedic weight-bearing restrictions, or to usual physiotherapy. The primary outcome will be lower-limb function measured using the Lower Extremity Functional Scale (LEFS). Secondary outcomes will include functional mobility, walking endurance, pain, knee and ankle range of motion, functional ambulation, walking-aid dependence, and adverse events. Outcomes will be assessed at baseline, post-intervention, and follow-up. The study aims to determine whether a standardized criteria-based rehabilitation approach can improve functional recovery following traumatic tibial fracture fixation.
Detailed description
### Detailed Intervention Prescription
Participants allocated to the intervention group will receive a structured criteria-based progressive loading and functional rehabilitation program for approximately 6-8 weeks, consisting of 2-3 supervised physiotherapy sessions per week in addition to an individualized home exercise program. Each supervised session will last approximately 45-60 minutes and will include an individualized combination of joint mobility, muscle strengthening, balance, gait, and functional training according to the participant's clinical status and stage of recovery.
The fundamental principle of the intervention is that progression will be determined by predefined clinical and functional criteria rather than postoperative time alone. All weight-bearing and loading activities will strictly follow the restrictions prescribed by the treating orthopedic or surgical team. The physiotherapist will not independently advance a participant beyond the medically permitted weight-bearing level.
Phase 1: Protection and Early Mobility
During the initial phase, rehabilitation will focus on protecting the surgical site, controlling symptoms, maintaining joint mobility, minimizing muscle weakness, and achieving safe basic mobility. Treatment will include patient education, appropriate positioning, pain and edema management, active or active-assisted knee and ankle range-of-motion exercises as clinically permitted, quadriceps activation, hamstring and gluteal exercises, ankle exercises, and straight-leg raising when appropriate. Muscle activation and mobility exercises will generally be performed for 2-3 sets of 10-15 repetitions according to the participant's tolerance.
Functional rehabilitation during this phase will include bed mobility, transfer training, sit-to-stand practice when appropriate, and instruction in the safe use of crutches or a walker according to the prescribed weight-bearing status. Participants will also receive an individualized home exercise program focusing primarily on mobility and muscle activation.
Progression from this phase will not occur simply because a predetermined number of postoperative weeks has elapsed. Progression will be considered when the participant demonstrates satisfactory wound and soft-tissue status, controlled pain and swelling, improving knee and ankle mobility, safe transfers, appropriate performance of the prescribed exercises, and adequate neuromuscular control.
Phase 2: Initial Loading and Gait Rehabilitation
This phase will begin once increased loading or weight-bearing has been medically permitted by the orthopedic or surgical team. Treatment will focus on gradually introducing the permitted load to the affected limb and restoring safe functional mobility.
Interventions will include controlled weight-shifting activities, weight-bearing practice within the prescribed limits, gait retraining using the appropriate walking aid, progressive lower-limb strengthening, sit-to-stand training, supported balance exercises, continued knee and ankle mobility exercises, and progressive walking practice. Strengthening exercises will generally be performed for 2-3 sets of approximately 8-15 repetitions, with resistance adjusted according to the participant's clinical status and ability to perform the movement with appropriate control.
Gait training will emphasize safe loading of the affected limb within the prescribed restriction, appropriate step pattern, correct use of the walking aid, balance, and progressive improvement in walking quality. Walking duration and distance will be increased gradually according to tolerance.
Progression will be considered when the participant can tolerate the currently prescribed loading level without clinically significant worsening of pain, swelling, or other symptoms; demonstrate controlled weight transfer; perform functional activities with satisfactory movement control; and walk safely using the prescribed assistive device. Advancement to a higher weight-bearing level will occur only when permitted by the treating orthopedic team.
Phase 3: Progressive Functional Loading
As greater weight-bearing is medically permitted, rehabilitation will progressively emphasize functional loading, lower-limb strength, balance, gait quality, and independence. Treatment will include progressive closed-chain exercises, functional strengthening, repeated sit-to-stand practice, step-up and step-down activities, balance and proprioceptive exercises, progressive walking, and gait-quality training.
Exercises will generally be prescribed for approximately 2-4 sets of 8-15 repetitions depending on the exercise, participant tolerance, and functional goal. The difficulty of exercises will be progressively increased by modifying resistance, repetitions, movement complexity, balance demands, walking distance, or the amount of upper-limb support rather than progressing according to time alone.
Reliance on crutches, a walker, or other upper-limb support will be reduced gradually when clinically appropriate and when consistent with the prescribed weight-bearing status. The participant must demonstrate adequate balance and safe gait before progressing to a less supportive walking aid.
Progression to advanced functional rehabilitation will require satisfactory tolerance of the current loading level, controlled symptoms, adequate movement quality, improving functional mobility and balance, safe ambulation, and medical permission for further loading.
Phase 4: Advanced Functional Rehabilitation
Once full weight-bearing is medically permitted, rehabilitation will focus on restoring independent mobility and preparing the participant for community, daily living, and occupational activities. Treatment will include independent gait training, stair negotiation, uneven-surface walking, functional squatting, advanced balance and proprioceptive exercises, progressive lower-limb strengthening, walking endurance training, community mobility activities, and activities of daily living.
Where relevant, rehabilitation will also include work-, household-, or activity-specific tasks based on the participant's individual functional requirements. Walking duration and distance will be progressively increased, and the participant will be encouraged to achieve safe mobility with the least restrictive walking aid or without an assistive device when appropriate.
Throughout all phases, the physiotherapist will assess pain, swelling, range of motion, functional performance, gait safety, exercise tolerance, and any adverse clinical response. Exercise intensity or loading will be reduced or temporarily withheld if the participant develops clinically significant worsening of pain or swelling, wound problems, loss of functional performance, or other signs requiring medical reassessment. Suspected fixation-related complications, wound complications, or other significant adverse events will be referred to the treating medical or surgical team.
The home exercise program will be individualized according to the participant's current rehabilitation phase. Mobility and muscle-activation exercises may be performed daily, while strengthening, balance, gait, and functional activities will be prescribed according to clinical tolerance and safety. Adherence to the home program and supervised physiotherapy sessions will be documented.
The main distinction between this intervention and usual physiotherapy is therefore not the individual exercises themselves. Participants receiving usual physiotherapy may also receive range-of-motion exercises, strengthening, gait training, balance exercises, walking-aid training, and functional exercises. In the intervention group, however, rehabilitation will follow a standardized criteria-based pathway in which advancement, regression, and functional progression are determined by predefined clinical and functional milestones while remaining within the weight-bearing restrictions established by the orthopedic team.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Criteria-Based Progressive Loading and Functional Rehabilitation | Experimental | Other: Criteria-Based Progressive Loading and Functional Rehabilitation ProgramParticipants assigned to the experimental arm will receive a structured criteria-based progressive loading and functional rehabilitation program for approximately 6-8 weeks, with 2-3 supervised physiotherapy sessions per week in addition to an individualized home exercise program. The program will progress through four rehabilitation phases according to predefined clinical and functional criteria rather than postoperative time alone. Phase 1 will focus on protection and early mobility and may include pain and edema management, positioning, knee and ankle range-of-motion exercises, quadriceps activation, hamstring and gluteal exercises, ankle exercises, bed mobility, transfer training, and safe use of walking aids. Phase 2 will introduce medically permitted loading through controlled weight shifting, weight-bearing practice, gait retraining, progressive strengthening, sit-to-stand training, supported balance exercises, and progressive walking. Phase 3 will emphasize progressive functi |
| Usual Physiotherapy | Active comparator | Other: Criteria-Based Progressive Loading and Functional Rehabilitation ProgramParticipants assigned to the control arm will receive the usual physiotherapy rehabilitation routinely provided at the participating rehabilitation centers following surgical fixation of traumatic tibial fractures. Usual physiotherapy may include pain and edema management, knee and ankle range-of-motion exercises, muscle strengthening, gait training, balance exercises, walking-aid training, functional exercises, progressive walking, and home exercise advice according to routine clinical practice and the individual needs of the participant. Weight-bearing and loading will follow the instructions provided by the treating orthopedic or surgical team. Unlike the experimental arm, progression of rehabilitation will not be guided by the standardized study-specific criteria-based progression algorithm. The number and duration of physiotherapy sessions and the principal interventions received will be documented throughout the study. |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (9 listed)
- Age ≥18 years.
- Traumatic unilateral tibial fracture involving the proximal tibia/tibial plateau, tibial shaft, or distal tibia.
- Treated with surgical fixation.
- Recruitment 2-8 weeks after the index fixation surgery.
- Medically and surgically stable and cleared by the treating team to participate in physiotherapy.
Key exclusion criteria (9 listed)
- Pathological fracture.
- Unstable fixation, fixation failure, or any orthopedic/medical contraindication to progressive rehabilitation.
- Active or uncontrolled infection requiring restriction or interruption of rehabilitation.
- Lower-limb amputation affecting functional assessment.
- Spinal cord injury or severe traumatic brain injury affecting mobility or ability to participate.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Criteria-Based Progressive Loading and Functional Rehabilitation ProgramParticipants will receive a structured Criteria-Based Progressive Loading and Functional Rehabilitation Program for 12 weeks, consisting of 2-3 supervised physiotherapy sessions per week plus an individualized home exercise program. Rehabilitation will progress through four phases: protection and early mobility; initial loading and gait rehabilitation; progressive functional loading; and advanced functional rehabilitation. Treatment will include pain and edema management, knee and ankle range-of-motion exercises, progressive lower-limb strengthening, weight-shifting and permitted weight-bearing practice, gait training, balance and proprioceptive exercises, sit-to-stand and step training, progressive walking, endurance training, and functional mobility activities. Progression will be based on predefined clinical and functional criteria rather than time alone and will remain within orthopedic weight-bearing restrictions. Participants will be followed for an additional 3 months after comp | Other | Criteria-Based Progressive Loading and Functional Rehabilitation, Usual Physiotherapy |
Primary outcome
Lower Extremity Functional Scale
Time frame: pre, 12 weeks post and 3 months follow up
The LEFS will be used to assess lower-limb functional status and the participant's difficulty performing everyday activities. The scale consists of 20 items, each scored from 0 to 4, producing a total score ranging from 0 to 80. Higher scores indicate better lower-extremity function. The primary endpoint will be the between-group difference in change in LEFS from baseline to completion of the intervention.
Timed Up and Go Test (TUG)
Time frame: pre, 12 weeks post and 3 months follow up
Functional mobility will be assessed using the TUG. Participants will stand from a chair, walk 3 meters, turn, walk back to the chair, and sit down. The total time required to complete the task will be recorded in seconds, with a shorter time indicating better functional mobility. The test will only be performed when medically appropriate according to the participant's weight-bearing status
Numeric Pain Rating Scale (NPRS)
Time frame: pre, 12 weeks post and 3 months follow up
Pain intensity will be measured using an 11-point numeric rating scale from 0 to 10, where 0 represents no pain and 10 represents the worst imaginable pain. Lower scores indicate less pain. Pain at rest and/or during functional activity will be documented according to the study assessment protocol
Functional Ambulation Category
Time frame: pre, 12 weeks post and 3 months follow up
The FAC will be used to classify the participant's level of functional walking independence and the amount of physical assistance required during ambulation. It is an ordinal scale ranging from 0 to 5, where 0 indicates inability to walk or the need for assistance from two or more people and 5 indicates independent ambulation. Higher scores indicate greater walking independence
2 secondary outcomes
ROM
Time frame: pre, 12 weeks post and 3 months follow up
Walking-Aid Dependence
Time frame: pre, 12 weeks post and 3 months follow up
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Sep 2026.
- Background: PubMed 10201543Binkley JM, Stratford PW, Lott SA, Riddle DL. The Lower Extremity Functional Scale (LEFS): scale development, measurement properties, and clinical application. North American Orthopaedic Rehabilitation Research Network. Phys Ther. 1999 Apr;79(4):371-83.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Criteria-Based Progressive Loading and Functional Rehabilitation Program in people with Tibial Fracture, run by Al-Azhar University at 1 site in Palestinian Territories.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 21 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Palestinian Territories. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mosab M Aldabbas, PhD (00972597451222, mosab.m.aldabbas@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Lower Extremity Functional Scale (time frame: pre, 12 weeks post and 3 months follow up). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07810478, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Sep 2026.