NCT07628374

Brief Summary

The aim of this study is to determine the comparative effects of sensorimotor training and dual-task training on propriocetion, balance, functional mobility and fall risk in stroke patients.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P50-P75 for not_applicable stroke

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable stroke

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress62%
Apr 2026Jul 2026

Study Start

First participant enrolled

April 20, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 1, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 5, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 5, 2026

Expected
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2026

Last Updated

June 5, 2026

Status Verified

June 1, 2026

Enrollment Period

3 months

First QC Date

June 1, 2026

Last Update Submit

June 1, 2026

Conditions

Keywords

Cognitive exercise, Dual-task, Proprioception, Rehabilitation, Sensorimotor exercise, Stroke.

Outcome Measures

Primary Outcomes (1)

  • Mini-BESTest Scale

    It is a tool to assess dynamic balance across four domains: anticipatory postural adjustments, reactive postural control, sensory orientation, and dynamic gait. It consists of 14 items, each scored from 0 to 2, with a maximum total score of 28. Higher scores indicate better balance performance. The test is sensitive to changes in individuals with neurological conditions, including stroke.

    8th week

Secondary Outcomes (1)

  • 6-minute Walk Test(6MWT)

    8th week

Study Arms (3)

Sensorimotor Training

ACTIVE COMPARATOR

Sensorimotor Training

Other: Sensorimotor Training

Dual-Task Training

EXPERIMENTAL

Dual-Task Training

Other: Dual-Task Training

Conventional Physical Therapy

ACTIVE COMPARATOR

Conventional Physical Therapy

Other: Conventional Physical Therapy

Interventions

Somatosensory Training(SMT), for 30 minutes, thrice a week for 8 weeks. Warm-up and cool down will be given.

Also known as: Sensroy Retraining/Re-education, Sensory Motor Training
Sensorimotor Training

Dual-Task Training, for 30 minutes, thrice a week for 8 weeks. Warm-up and cool down will be given.

Dual-Task Training

Conventional Physical Therapy, for 30 minutes, thrice a week for 8 weeks. Warm-up and cool down will be given.

Conventional Physical Therapy

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • A diagnosis of stroke; ≥6 months after stroke onset
  • Able to walk independently for at least 10 minutes
  • Mini-BESTest score ≤21 indicating balance impairment.
  • MoCA score ≥21 to confirm adequate cognitive function

You may not qualify if:

  • Severe musculoskeletal conditions (e.g., advanced osteoarthritis, recent fractures) that significantly affect mobility or balance.
  • Significant receptive or expressive aphasia
  • Unstable heart or lung conditions preventing exercise.
  • Active psychiatric disorders (e.g., major depression, schizophrenia)
  • Not community-dwelling before the stroke event
  • Involved in similar rehab or studies within the last 3 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

DHQ Rajanpur

Rajanpur, Punjab Province, 33500, Pakistan

RECRUITING

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Sabiha Arshad

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Masking Details
Randomized for RCT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 1, 2026

First Posted

June 5, 2026

Study Start

April 20, 2026

Primary Completion (Estimated)

July 5, 2026

Study Completion (Estimated)

July 20, 2026

Last Updated

June 5, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations