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NCT Number: NCT07697794

Environmental-perturbation Balance Training Improves Functional Outcomes in Patients With Subacute Stroke

This study innovatively proposes an "environment-perturbation balance training (E-PBT)" intervention, which delivers stable, graded environmental perturbations to keep the challenges within the manageable range. This approach can significantly reduce fear, align with the psychological characteristics of subacute stroke patients, and improve training engagement and safety, thereby filling the current research gap that has insufficiently addressed subacute patients and those with moderate-to-low functional levels. By altering the size and angle of the support surface, this training heightens patients' alertness and psychological adaptability, prompting them to actively integrate sensory information and adjust motor strategies. In turn, this can more effectively reshape internal model of balance control and facilitate genuine neuroadaptive learning in the brain. Moreover, this training more closely mimics real-life fall scenarios, with the aim of directly cultivating the proactive postural control and strategic decision-making abilities required in daily living.

This study aims to systematically evaluate the efficacy of this E-PBT intervention on functional recovery in patients during the subacute stage of stroke through a prospective randomized controlled trial, and to explore its potential effects on balance ability, activities of daily living, and overall functional outcomes, thereby providing a more effective and clinically translatable new strategy for post-stroke rehabilitation.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Shenyang First People's Hospital

Shenyang, Liaoning, 110041, China

Location contact

Hong Wang, bachelor's degree

CONTACT

[email protected]

02431956718

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with stroke according to the International Symposium on Cerebral Vascular Disease criteria, with definite confirmation by imaging modalities such as computed tomography (CT) or magnetic resonance imaging (MRI).
  • First-ever or recurrent cerebral hemorrhage or cerebral infarction. According to the Guidelines for the Early Management of Patients with Acute Ischemic Stroke: A Guideline for Healthcare Professionals from the American Heart Association/American Stroke Association and the Chinese Guidelines for Early Rehabilitation of Stroke, rehabilitation can be initiated once the patient's condition is stable (vital signs are stable and no further progression of symptoms and signs).
  • Total NIHSS score between 5 and 20 (inclusive) prior to randomization, with a lower limb motor score ≥2.
  • Presence of balance dysfunction, with a miniBESTest total score ≤12.
  • Good compliance with rehabilitation therapy and no contraindications to active training.
  • Age between 18 and 85 years.
  • The subject or their legal representative is able and willing to provide written informed consent.

Exclusion criteria

  • History of prior cerebral hemorrhage or cerebral infarction with residual significant limb dysfunction.
  • Severe cognitive impairment or sensory aphasia that precludes communication and cooperation with treatment.
  • Concomitant severe cardiopulmonary, hepatic, or renal insufficiency, or other serious medical diseases.
  • Presence of neurological or musculoskeletal disorders affecting balance function prior to stroke onset.
  • Uncontrolled severe hypertension or diabetes mellitus.
  • Active bleeding or deep vein thrombosis.
  • Current participation in another clinical trial or rehabilitation program that may affect the results of this study.
  • Any other condition that may interfere with the outcomes of this study.
  • History of limb amputation affecting bilateral coordination or independent walking ability.
  • Pregnancy.

Treatment and study plan

Environmental-perturbation balance training

Behavioral

The core principle of this training is to deliver standardized, controllable environmental perturbations tailored to the patient's functional level. All perturbations will be administered under safe conditions, following a stepwise "challenge-adapt-rechallenge" progression principle, with the aim of maximizing the patient's active postural control strategies and neuromuscular adaptation, thereby improving balance function and ultimately facilitating the patient's return to home and community life.

Conventional rehabilitation training

Behavioral

Participants in the control group will receive conventional rehabilitation training based on the principles of neuro-developmental therapy (NDT) and motor relearning programme (MRP). The training will include static and dynamic sitting and standing balance, weight shifting, single-leg stance, weight-bearing exercises, core stabilization training, straight-line walking on firm, level ground, and step up and down exercises.

Primary outcomes

  1. The incidence of good functional outcomes after treatment (mRS)

    Time frame: At 90 days post-stroke

    The primary outcome of this study is the improvement in neurological functional outcome at 90 days post-stroke, as measured by the modified Rankin Scale (mRS). The mRS is a 7-level ordinal scale ranging from 0 to 6, with higher scores indicating greater disability. For clinical interpretability and statistical analysis, the mRS will be dichotomized as follows: a favorable outcome is defined as an mRS score of ≤ 3 (indicating the ability to walk independently or with minimal assistance), and an unfavorable outcome is defined as an mRS score of ≥ 4 (indicating inability to walk independently and requiring assistance in daily activities). At 90 days (±7 days) after stroke, the mRS score will be assessed by trained evaluators who are blinded to group allocation, through face-to-face interviews or telephone follow-ups. The primary comparison will be the difference in the proportion of favorable outcomes (i.e., mRS ≤ 3) between the two groups.

Secondary outcomes

  1. Shift analysis of the modified Rankin Scale (mRS)

    Time frame: At 90 days post-stroke

    In contrast to the primary binary outcome, the shift analysis will be able to capture the treatment effect of E-PBT on the functional prognosis of post-stroke patients more sensitively, by avoiding information loss associated with the use of a fixed dichotomization threshold.

  2. Modified Barthel Index

    Time frame: At 90 days post-stroke

    Activities of daily living will be assessed using the Modified Barthel Index (MBI), which consists of 10 items with a total score ranging from 0 to 100. Higher scores indicate greater independence in daily living. The assessment will be administered through a structured interview to capture the patient's actual performance during the preceding week.

  3. mini-BESTest

    Time frame: Baseline and 90 days post-stroke

    Balance function will be assessed using the mini-Balance Evaluation Systems Test (mini-BESTest), which consists of 14 items with a total score ranging from 0 to 28. Higher scores indicate better dynamic balance ability. This scale has been demonstrated to have good responsiveness to changes in balance function in stroke patients.

  4. Overall Stability Index

    Time frame: At 90 days post-stroke

    The Overall Stability Index will be measured using the balance function training and assessment system (XY-PH-V) to quantify the displacement of the center of pressure (COP) during static standing. A lower OSI value indicates better postural control ability. Since the majority of participants are unable to stand independently at baseline, this outcome will only be collected after the completion of the intervention.

  5. Trunk Impairment Scale

    Time frame: Baseline and 90 days post-stroke

    Trunk function will be assessed using the Trunk Impairment Scale (TIS), which consists of three subscales: static sitting balance, dynamic sitting balance, and coordination. The total score ranges from 0 to 23, with higher scores indicating better trunk control.

  6. Scale for Contraversive Pushing

    Time frame: Baseline and 90 days post-stroke

    The presence of pusher syndrome will be evaluated using the Scale for Contraversive Pushing (SCP). The SCP comprises the following three items: (1) asymmetry of posture, (2) abduction or extension of the non-paretic limb, and (3) resistance to passive correction of posture. Pusher syndrome is considered to be present when the score for each of the three SCP items is > 0.

  7. Timed Up and Go Test

    Time frame: At 90 days post-stroke

    The TUG will record the time (in seconds) required for the participant to rise from a chair, walk 3 meters, turn around, return, and sit down again. Shorter times indicate better mobility. The use of assistive devices is permitted during the test, but physical assistance from others is not allowed.

  8. b) 6-Minute Walk Test

    Time frame: At 90 days post-stroke

    The 6MWT will record the total distance (in meters) that the participant can walk as far as possible within 6 minutes. If the test is terminated early due to fatigue or safety concerns, the actual distance walked and the reason for termination will be recorded.

  9. Fugl-Meyer Assessment for Lower Extremity

    Time frame: At 90 days post-stroke

    Lower extremity motor function will be assessed using the Fugl-Meyer Assessment for Lower Extremity (FMA-LE). The scale consists of 17 items, with a total score ranging from 0 to 34. Higher scores indicate better lower limb motor function.

Study contacts

Contact information is provided by the study sponsor or research team.

Hong Wang, bachelor's degree

CONTACT

[email protected]

02431956718

Sponsors and collaborators

Lead sponsor

First People's Hospital of Shenyang

Other

Registry information

Official study title

Environmental-Perturbation Balance Training Improves Functional Outcomes in Patients With Subacute Stroke: A Prospective Randomized Controlled Trial

Acronym: E-PBT

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 13, 2026
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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