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Not yet recruitingNCT07791485Updated Aug 28, 2026

Postoperative Rehabilitation in Adolescent Idiopathic Scoliosis

An interventional study of Exercise-Based Rehabilitation Program in Surgery, Rehabilitation and Scoliosis; Adolescence, sponsored by Marmara University. Not yet recruiting. Open to participants aged 10 Years to 20 Years. Per ClinicalTrials.gov, last updated 2026-08-28.

Sponsored by Marmara University · Not applicable, Interventional, and Treatment

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Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
10 Years to 20 Years
Sex
All
01

Study summary

Adolescent idiopathic scoliosis (AIS) is a three-dimensional spinal deformity occurring in growing individuals. In cases with progressive curvature, posterior spinal fusion and instrumentation (PSF) is considered the gold-standard surgical treatment for correcting the deformity and stabilizing the spine. Although surgery provides correction of the deformity, the loss of motion in the fused spinal segments may alter trunk biomechanics, potentially affecting postural control, balance mechanisms, and plantar pressure distribution.

Although several studies have investigated balance and postural control parameters in individuals with AIS, no study has been identified that objectively examines the effects of postoperative rehabilitation programs on stabilometric balance, postural control, and plantar pressure distribution following PSF surgery.

This study aims to investigate the effects of an exercise-based rehabilitation program on stabilometric balance, postural control, and plantar pressure distribution in individuals with AIS who have undergone PSF surgery. This randomized controlled trial is planned to include at least 42 individuals with AIS who have undergone PSF surgery and are being followed by the Department of Neurosurgery at Marmara University. Participants will be randomly assigned to an intervention group or a control group. The intervention group will participate in an exercise-based rehabilitation program consisting of two sessions per week for eight weeks. Consistent with routine practice, the control group will not participate in a structured rehabilitation program.

Postural control, stabilometric balance, and plantar pressure distribution will be assessed using a stabilometric and baropodometric platform system. Assessments will be conducted before and after the rehabilitation period. The findings are expected to contribute to the scientific evidence regarding postoperative rehabilitation approaches. The results may also guide clinicians in planning exercise-based rehabilitation programs following scoliosis surgery and provide patients and their families with useful information regarding the postoperative recovery process.

Read the detailed description

Scoliosis is a complex three-dimensional deformity characterized by a lateral deviation of the spine of at least 10 degrees in the coronal plane (Choudhry et al., 2016). Idiopathic scoliosis is a structural form of scoliosis for which no specific etiology has been identified. When it develops between the onset of puberty and the closure of the growth plates, it is classified as adolescent idiopathic scoliosis (AIS) (Winter, 1994; Weinstein et al., 2008).

Current treatment options for scoliosis include observation, bracing, and surgical intervention. Selection of the most appropriate treatment approach depends on factors such as the patient's age, menarcheal status, curve location and magnitude, and risk of progression (Zhang et al., 2020). Although skeletally immature children with curves reaching 40-50 degrees are generally considered candidates for surgical treatment, other factors-including curve pattern, rate of progression, the presence of additional deformities, and failure to respond to conservative treatment-may also influence the decision to perform surgery (Bridwell, 1999; Kim et al., 2009; Pourfeizi et al., 2014). Among the various surgical procedures used to treat scoliosis, posterior spinal fusion and instrumentation (PSF) is the most commonly used approach and is regarded as the gold-standard surgical technique in the literature (Lonner et al., 2007). This technique eliminates motion in the involved spinal segments by creating a fusion to correct the deformity, achieve a balanced spine, and prevent further curve progression (Upasani et al., 2015).

Alterations in balance control, postural stability, and postural sway parameters have been reported in individuals with AIS due to the three-dimensional spinal deformity. Impairments in sensorimotor integration mechanisms involving the trunk and changes in plantar pressure distribution have also been reported (Beaulieu et al., 2009; Sahli et al., 2013; Karimi et al., 2016; Dufvenberg et al., 2018). Following surgical correction, the elimination of motion in certain spinal segments may increase loading on the remaining mobile segments, leading to changes in trunk biomechanics and new adaptations in postural control mechanisms. However, the limited evidence regarding the effects of these changes and adaptations in individuals with scoliosis remains inconsistent. Previous studies have reported postoperative reductions in spinal flexibility and mobility, as well as chronic pain (Danielsson et al., 2001; Engsberg et al., 2003; Maruyama et al., 2008), decreased trunk muscle endurance (Danielsson et al., 2006), adverse effects on balance- and postural control-related parameters, or a lack of improvement in these parameters following surgery (McCance et al., 1998; de Santiago et al., 2013; Osuka et al., 2023).

Studies addressing the postoperative period have suggested that physiotherapist-supervised rehabilitation programs may be important for preventing secondary spinal problems and supporting postoperative recovery (Weiss, 2002; Laurentowska et al., 2009; Bazancir et al., 2023; Çetinkaya et al., 2025). Nevertheless, only a limited number of studies have investigated postoperative rehabilitation in individuals with AIS. Laurentowska et al. reported that a four-week endurance-based rehabilitation program initiated one to three years after surgery significantly improved exercise capacity and emphasized that rehabilitation should continue after spinal fusion in individuals with scoliosis (Laurentowska et al., 2009). Weiss demonstrated that a pain-management-based inpatient rehabilitation program could reduce chronic pain in patients who had undergone surgery at least 10 years earlier (Weiss, 2002). Short-term inpatient rehabilitation programs implemented after scoliosis surgery have also been reported to support postoperative recovery and improve quality of life (Bazancir et al., 2023). In addition, a physiotherapist-supervised telerehabilitation program initiated from the sixth postoperative month was reported to improve trunk endurance and flexibility and positively affect quality of life (Çetinkaya et al., 2025). Although these studies have addressed postoperative rehabilitation approaches, there remains a notable lack of research examining the effects of rehabilitation on biomechanical variables such as postural control mechanisms, stabilometric balance parameters, and plantar pressure distribution following surgery.

Changes in postural control and balance mechanisms may affect individuals' activities of daily living and their participation in social and physical activities. Participation in physical activity and social life is particularly important during adolescence because of its contribution to overall health and quality of life. Therefore, it is important to investigate postoperative rehabilitation approaches aimed at supporting functional capacity and facilitating the reorganization of postural control mechanisms. Further research is also needed to establish evidence-based rehabilitation programs that support the biomechanical adaptation of the fused spine and the postoperative recovery process.

Accordingly, this study aims to investigate the effects of an exercise-based postoperative rehabilitation program on stabilometric balance, postural control, and static plantar pressure distribution in individuals who have undergone PSF surgery for AIS, using objective biomechanical assessment methods. The findings are expected to contribute to the development of postoperative rehabilitation approaches and to support individuals' functional independence and quality of life. The results are also expected to provide evidence regarding the effectiveness of the exercise program and to offer guidance for clinicians working in this field, as well as for patients and their families.

02

Conditions studied

  • Surgery
  • Rehabilitation
  • Scoliosis; Adolescence

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Keywords

  • adolescent idiopathic scoliosis
  • postoperative rehabilitation
  • scoliosis surgery
03

In context

Scoliosis

660 studies on the registry are indexed under Scoliosis; 186 are open to participants now.

This study's planned enrollment of 42 is close to the median of 45 across 386 interventional studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

Marmara University is the lead sponsor of 599 studies on the registry; 138 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 20 Years
Sexes eligible
All
Accepts healthy volunteers
No

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.

Inclusion criteria

  • Aged 10 years or older
  • Diagnosed with adolescent idiopathic scoliosis
  • Having undergone posterior spinal fusion and instrumentation between 6 months and 3 years before enrollment

Exclusion criteria

Exclusion Criteria:

  • Having undergone anterior spinal fusion and instrumentation, combined anteroposterior spinal fusion and instrumentation, thoracoscopic vertebral body tethering, or vertebral body stapling
  • A history of previous spinal surgery other than the current posterior spinal fusion procedure
  • The presence of a severe neuromuscular, rheumatological, or orthopedic condition accompanying scoliosis
  • The presence of a congenital deformity, such as leg-length discrepancy, limb agenesis, or limb hypoplasia
  • Current participation in another physiotherapist-supervised rehabilitation program
  • Inadequate biological healing based on radiographic assessment or being considered unsuitable for participation by the treating physician
  • Inability to perform the assessments or interventions required by the study or inability to cooperate with study procedures
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
42 participants (estimated)

Study arms

  • Experimental
    Treatment Group

    Participants who are at least six months post-surgery and are periodically invited by their physician for routine postoperative follow-up examinations, including radiological assessment and physical examination, will participate in an exercise-based rehabilitation program. The program will consist of 16 sessions delivered twice weekly for eight weeks, with each session lasting approximately 60 minutes.

    Other: Exercise-Based Rehabilitation Program

  • No intervention
    Control Group

    Participants who are at least six months post-surgery and are routinely invited by their physician for radiological assessment and physical examination at six-month intervals will not participate in any structured rehabilitation program beyond the periodic follow-up and recommendations provided as part of routine postoperative care. Participants assigned to this group will be offered the opportunity to participate in the exercise-based rehabilitation program after completing the study if they wish.

Interventions

  • OtherExercise-Based Rehabilitation Program

    Participants in the experimental group will receive a supervised exercise-based rehabilitation program consisting of 16 sessions delivered twice weekly for eight weeks. Each session will last approximately 60 minutes and will be supervised by a physiotherapist. The program will focus on core muscle control, spinal mobility, and dynamic stabilization and will begin with face-to-face patient education. Exercise equipment will be provided by the researchers, and a five-minute rest period will be allowed when requested. On days without supervised sessions, participants will perform the prescribed exercises at home for approximately 20 minutes and record their adherence in an exercise diary, which will be reviewed during the supervised sessions.

06

What researchers measure

Primary outcomes

  1. Change in Center of Pressure Sway

    Center of pressure (CoP) sway during quiet standing will be assessed using the FreeMed® stabilometric platform and FreeStep® software. Participants will stand barefoot with their feet shoulder-width apart, arms relaxed at their sides, and eyes focused on a fixed point during a 25-second recording. Three measurements will be performed, and the mean value will be used for analysis. Lower values indicate less postural sway.

    Time frame: Baseline and immediately after the 8-week intervention

  2. Change in Center of Pressure Sway Velocity

    Center of pressure sway velocity during quiet standing will be assessed using the FreeMed® stabilometric platform and FreeStep® software during a 25-second recording. Three measurements will be performed under the same standardized conditions, and the mean value will be used for analysis. Lower values indicate slower postural sway and better postural stability.

    Time frame: Baseline and immediately after the 8-week intervention

  3. Change in Center of Pressure Stability Ellipse Area

    The stability ellipse area of the center of pressure trajectory during quiet standing will be assessed using the FreeMed® stabilometric platform and FreeStep® software during a 25-second recording. Three measurements will be performed, and the mean value will be used for analysis. A smaller ellipse area indicates less postural sway.

    Time frame: Baseline and immediately after the 8-week intervention

  4. Change in Directional Center of Pressure Sway

    Anteroposterior and mediolateral center of pressure sway during quiet standing will be assessed using the FreeMed® stabilometric platform and FreeStep® software during a 25-second recording. Anteroposterior and mediolateral sway will be recorded as separate parameters. Three measurements will be performed, and the mean values will be used for analysis. Lower values indicate less directional postural sway.

    Time frame: Baseline and immediately after the 8-week intervention

Secondary outcomes

  1. Change in Static Plantar Load Distribution

    Static plantar load distribution during quiet standing will be assessed using the FreeMed® baropodometric platform and FreeStep® software. The percentages of load distributed between the right and left feet, forefoot and rearfoot, and medial and lateral plantar regions will be recorded. Three measurements will be performed, and the mean values will be used for analysis. Values closer to an even distribution indicate greater load symmetry.

    Time frame: Baseline and immediately after the 8-week intervention

  2. Change in Plantar Contact Area

    The plantar contact area of the right and left feet during quiet standing will be assessed using the FreeMed® baropodometric platform and FreeStep® software. Contact area will be recorded separately for each foot. Three measurements will be performed, and the mean values will be used for analysis.

    Time frame: Baseline and immediately after the 8-week intervention

  3. Change in Postural Alignment

    Postural alignment will be assessed using the video analysis system integrated with the FreeMed® platform. Trunk inclination, pelvic tilt, and shoulder tilt will be recorded as separate postural alignment parameters. Three measurements will be performed using the same standardized protocol, and the mean values will be used for analysis. Values closer to neutral alignment indicate less postural asymmetry.

    Time frame: Baseline and immediately after the 8-week intervention

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Apr 2027, 7 months later.

Of 223 non-industry interventional studies with no phase under Scoliosis, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 58. This study's planned 7 months is below that.

Counting every sponsor, half of 233 studies reached it within 22 months; a quarter within 8 and three quarters within 60.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 22, 2026
First posted
Aug 28, 2026
StartEst.
Sep 1, 2026
Primary completionEst.
Apr 1, 2027
CompletionEst.
Jun 1, 2027
Last update
Aug 28, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07791485
Lead sponsor
Marmara University
Responsible party
Sponsor
First posted
Aug 28, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Apr 1, 2027 (estimated)
Completion
Jun 1, 2027 (estimated)
Last update
Aug 28, 2026

Study contacts

İrem Çetinkaya, PhD
Contact
iremkaranki@gmail.com
5548056805
İrem Çetinkaya, PhD
principal investigator · Marmara University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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