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Chronic Stroke PatientsNCT07139002

Combined Effect of Sensory Training With Bobath Therapy in Patients With Chronic Stroke

A study testing Bobath Therapy and Sensory Training in people with Chronic Stroke Patients, run by Riphah International University at 1 site in Pakistan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Chronic stroke causes moderate to severe impairments in proprioception, balance, and motor functions, which can impact upon an individual's ability to perform activities of daily living, leading to reduced quality of life and increased dependency. Read more about this study

Who is it for?
Ages 45 to 60 years
Conditions the study is for
Chronic Stroke Patients
What is being tested?
Bobath Therapy and Sensory Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 sitePakistan
Study dates
1 Jan 2025to 30 Nov 2025
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 45 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Both male and female included.
  • Age group: 45 years to 60 years.
  • Participants diagnosed with chronic stroke 6 months to 2 years.
  • Mini-Mental State Examination (MMSE) score of 24 or higher.
  • Cannot maintain balance for 30 seconds.
  • Ambulate independently for 7 meters.

Who cannot join

  • Participants having conditions other than chronic stroke (Parkinson's disease, Alzheimer's disease, orthopedic pathological condition, etc.).
  • Participants having any visual, vestibular, or auditory impairment.
  • Participants having any muscular injuries in the previous 6 months.
  • Participants with a history of fracture in the previous 6 months.
  • Participants with a history of mental illness.
  • Participants with cardiovascular complications.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Asrar Yousaf, M.phill contact

+923004099505

Asrar.yousaf@riphah.edu.pk

Pakistan1 site, 1 recruiting
  • Ittefaq Hospital (Trust), Lahore

    Lahore, Punjab Province, 54000

    Noshaba Dilshad, MSPT-NM, +923335826644, noshabadilshad@gmail.com

    Noshaba Dilshad, MSPT-NM

    Recruiting

Other trials in Pakistan

About this study

Official title: Combined Effect of Sensory Training With Bobath Therapy on Proprioception, Balance, and Motor Function in Patients With Chronic Stroke

Chronic stroke causes moderate to severe impairments in proprioception, balance, and motor functions, which can impact upon an individual's ability to perform activities of daily living, leading to reduced quality of life and increased dependency. Proprioception, or detecting the body's position in open space, is important for balance and coordinated movement. One therapy uses traditional rehabilitation methods like Bobath theory to increase motor functions, aiming to utilize sensory and movement facilitation. Nonetheless, combining sensory and Bobath therapy could lead to superior outcomes by simultaneously addressing both the proprioceptive deficit and motor skills. The purpose of this project is to explore the combined effect of sensory training and Bobath therapy on proprioception, balance, andmotor function in chronic stroke survivors.

Read the detailed description

This randomized controlled trial study will take place at Ittefaq (Trust) Hospital, Lahore, with a sample size of 40 participants. Eligible participants will include individuals who are 6 months to 2 years old chronic stroke patients (age group 45 years to 60 years), possess a Mini-Mental State Examination (MMSE) score of 24 or higher, and can provide informed consent. Participants will be selected using nonprobability convenience sampling by using online randomizing tools. The participants will be randomly divided into groups (20 each). The study group will be subjected to combined sensory training and Bobath therapy. The duration of the intervention will be eight weeks, with three sessions per week aimed at improving proprioceptive awareness and motor function. Proprioception will be assessed using the proprioception assessment tool (PAT), joint position sense, and the Romberg test, while balance will be determined using the Berg Balance Scale. The Fugl-Meyer Assessment will be used to measure motor function. The first assessments will be the baseline assessments, done before the intervention, after which a follow-up will be done to measure the efficacy of the combined approach. Statistical analyses will be conducted to assess differences in outcomes between the two groups, helping to determine the effectiveness of combining sensory training with balance and motor function interventions in chronic stroke patients. The findings aim to contribute to the understanding of rehabilitation strategies for this population. Data analysis will be performed by using SPSS 26 software.

Being tested
Bobath Therapy, Sensory Training
Keywords
Bobath Therapy, Sensory training, Chronic Stroke, Balance, Motor function, Proprioception

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Bobath TherapyOther

    The group will repeat 10 exercises (facilitated rolling, sitting balance exercises, weight shifting in standing, functional sit-to-stand, stepping practice, reaching activities, wall slides, therapeutic ball exercises, stair climbing practice, and breathing and relaxation techniques) for 8 weeks.

  • Sensory TrainingOther

    The group will repeat 9 exercises (texture discrimination, shape, size, and discrimination, tactile recognition, proprioception training, temperature differentiation, tactile localization, sensory mapping, sensory training through functional activities, and tabletop sensory exercises) for 8 weeks.

Study groups in NCT07139002
Study groupRoleWhat they receive
Bobath TherapyOtherThe group will repeat 10 exercises (facilitated rolling, sitting balance exercises, weight shifting in standing, functional sit-to-stand, stepping practice, reaching activities, wall slides, therapeutic ball exercises, stair climbing practice, and breathing and relaxation techniques) for 8 weeks.
Receives: Other: Bobath Therapy
Sensory Training with Bobath TherapyExperimentalThe group will repeat 9 exercises (texture discrimination, shape, size, and discrimination, tactile recognition, proprioception training, temperature differentiation, tactile localization, sensory mapping, sensory training through functional activities, and tabletop sensory exercises) with Bobath Therapy for 8 weeks.
Receives: Other: Bobath Therapy; Other: Sensory Training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Romberg test

    Romberg test is popular for assessing proprioception

    Measured: 4 weeks

  2. Joint Position Sense Test

    Joint Position Sense Test is used for assessing proprioception

    Measured: 4 weeks

  3. Berg Balance scale

    Berg Balance scale is popular for assessing balance

    Measured: 4 weeks

  4. Timed up and go test

    Timed up and go test is popular for assessing balance

    Measured: 4 weeks

  5. Fugl-Meyer Assessment Tool

    Fugl-Meyer Assessment Tool is specific tool that evaluates motor functioning, balance, sensation, and joint functioning in stroke patients

    Measured: 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Aug 2025
  2. Study start1 Jan 2025
  3. Primary completion15 Sep 2025 (estimated)
  4. Study completion30 Nov 2025 (estimated)

Resources

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
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07139002
Sponsor's protocol ID
REC/RCR&AHS/24/0281
Status last verified
Aug 2025
First submitted
18 Aug 2025
Last updated
24 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Bobath Therapy and Sensory Training in people with Chronic Stroke Patients, run by Riphah International University at 1 site in Pakistan.

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 6 inclusion and 6 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 24 Aug 2025. 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 Pakistan. 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 Asrar Yousaf, M.phill (+923004099505, Asrar.yousaf@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Romberg test (time frame: 4 weeks). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 24 Aug 2025.

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