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NCT Number: NCT07467915

Combined Mirror Therapy and Soft Robotic Glove for Hand Recovery After Stroke

Post-stroke hemiplegia frequently results in impaired upper limb function, which significantly affects independence and quality of life. Various rehabilitation approaches have been developed to improve motor recovery, including mirror therapy and robotic-assisted training. Mirror therapy uses visual feedback to stimulate neural plasticity and enhance motor recovery, while soft robotic gloves assist repetitive hand movements and facilitate functional training.

This randomized controlled trial aims to investigate the effect of combining mirror therapy with a soft robotic glove on hand function recovery in patients with post-stroke hemiplegia. Participants will be randomly assigned to different intervention groups receiving mirror therapy, soft robotic glove training, combined therapy, or conventional rehabilitation.

The primary outcome will assess improvement in upper limb motor function using validated clinical assessment tools. Secondary outcomes will evaluate functional hand performance and activities of daily living. The findings of this study may contribute to improving rehabilitation strategies for stroke survivors and provide evidence for integrating innovative rehabilitation technologies into clinical practice.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Stroke is one of the leading causes of long-term disability worldwide and commonly results in upper limb motor impairment. Recovery of hand function is essential for improving independence in activities of daily living. However, rehabilitation of the affected upper limb remains a major challenge in stroke management.

Mirror therapy is a rehabilitation technique that provides visual feedback by reflecting movements of the unaffected limb in a mirror, creating the illusion that the affected limb is moving normally. This approach is believed to promote cortical reorganization and enhance motor recovery. In recent years, robotic-assisted rehabilitation devices, including soft robotic gloves, have been developed to provide repetitive, task-specific training and facilitate motor relearning.

Soft robotic gloves are wearable assistive devices designed to support hand movements and enable repetitive practice of grasping and releasing tasks. These devices provide controlled assistance during rehabilitation exercises and may enhance the intensity and effectiveness of therapy.

This study is designed as a randomized controlled trial to evaluate the effectiveness of combining mirror therapy with soft robotic glove training in improving hand function among patients with post-stroke hemiplegia. Eligible participants will be randomly assigned to intervention groups receiving mirror therapy, soft robotic glove training, combined therapy, or conventional rehabilitation.

The intervention program will be delivered over a structured rehabilitation period, and clinical assessments will be conducted at baseline and after completion of the intervention. Outcome measures will focus on upper limb motor recovery, hand function performance, and functional independence.

The results of this study are expected to provide evidence regarding the effectiveness of integrating mirror therapy with robotic-assisted rehabilitation approaches for improving upper limb recovery after stroke. This may support the development of more effective rehabilitation protocols for patients with post-stroke hemiplegia.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Adults aged 18-70 years with first-ever ischemic or hemorrhagic stroke confirmed by imaging (CT or MRI)

Moderate upper limb motor impairment (Fugl-Meyer Assessment Upper Extremity [FMA-UE] score 20-50)

Ability to follow simple instructions (Six-Item Cognitive Impairment Test, 6CIT)

Ability to sit independently for at least 30 minutes

Medically stable and cleared to participate in rehabilitation interventions

Willingness to provide informed consent and adhere to the study protocol

Exclusion criteria

Severe upper limb spasticity (Modified Ashworth Scale ≥ 3)

Cognitive or psychiatric disorders interfering with participation

Other neurological or musculoskeletal conditions affecting upper limb function (e.g., Parkinson's disease, multiple sclerosis, fractures)

Prior exposure to intensive Mirror Therapy or Soft Robotic Gloves

Visual impairment that cannot be corrected with glasses or contact lenses

Uncontrolled cardiovascular or other medical conditions that would prevent safe participation

Treatment and study plan

conventional rehabilitation

Other

Standard rehabilitation therapy focused on improving upper limb function in individuals with stroke

Mirror Therapy

Other

A rehabilitation technique using a mirror to create a visual illusion of movement in the affected limb to improve motor recovery after stroke.

Soft Robotic Glove

Device

A wearable soft robotic glove designed to assist hand movement and facilitate motor recovery in individuals with stroke

Mirror Therapy plus Soft Robotic Glove

Combination Product

Participants receive a combined intervention consisting of mirror therapy and soft robotic glove training

Primary outcomes

  1. Upper Limb Motor Function (Fugl-Meyer Assessment for Upper Extremity, FMA-UE)

    Time frame: Baseline, 4 weeks during intervention, immediately post-intervention (6 weeks), and 3-month follow-up.

    Assesses motor recovery of the affected upper limb following stroke, including voluntary movement, coordination, and reflex activity using a standardized stroke-specific motor scale. Scores range from 0 to 66, with higher scores indicating better motor recovery and motor performance.

  2. Functional Use of Affected Limb (Functional Test of Upper Limb Hemiplegia - Hong Kong, FTHUE-HK)

    Time frame: Baseline, 4 weeks during intervention, immediately post-intervention (6 weeks), and 3-month follow-up

    Evaluates functional use of the affected upper limb in individuals with hemiplegia through hierarchical task performance. Scores range from Level 1 (no active movement) to Level 7 (advanced functional hand use), with higher levels indicating greater functional recovery.

Other outcomes

  1. Activities of Daily Living (Katz Index of Independence in ADL)

    Time frame: Baseline, 4 weeks, post-intervention, 3-month follow-up

    Measures the participant's ability to independently perform six basic self-care activities including bathing, dressing, toileting, transferring, continence, and feeding. Scores range from 0 to 6, with higher scores indicating greater independence in activities of daily living.

  2. Upper Limb Spasticity (Modified Ashworth Scale, MAS)

    Time frame: Baseline, 4 weeks, post-intervention, 3-month follow-up

    Assesses muscle spasticity in the affected upper limb by grading resistance during passive soft-tissue stretching. Scores range from 0 to 4, where higher scores indicate increased muscle tone and greater spasticity.

  3. Cognitive Screening (Six-Item Cognitive Impairment Test, 6CIT)

    Time frame: Baseline

    A brief screening tool used to assess cognitive status prior to study participation, including orientation, memory, and attention. Scores range from 0 to 28, with higher scores indicating greater cognitive impairment.

  4. Visual Acuity (Snellen Chart)

    Time frame: Baseline

    Evaluates visual acuity to ensure participants can adequately perform mirror-based visual feedback during therapy. Visual acuity is measured using the standard Snellen fraction (e.g., 6/6 to 6/60), where better vision corresponds to higher visual acuity.

Study contacts

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

Mohammed Hindi Jaryan, PhD Candidate

CONTACT

[email protected]

+9647808046480

Sponsors and collaborators

Lead sponsor

University of Baghdad

Other

Registry information

Official study title

Effect of Combining Mirror Therapy With Soft Robotic Glove on Hand Function Recovery in Post-Stroke Hemiplegic Patients: A Randomized Controlled Trial

Acronym: MT-SRG

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 12, 2026
Registry last updated
May 13, 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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