NCT07635069

Brief Summary

The objective of this study was to evaluate the cognitive effectiveness of somatotherapy and occupational therapy in post-stroke patients by measuring their cognitive potential outcomes using the Montreal Cognitive Assessment (MoCA) test.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2023

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

January 3, 2023

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 25, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 25, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

May 8, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

June 9, 2026

Completed
Last Updated

June 9, 2026

Status Verified

June 1, 2026

Enrollment Period

3 years

First QC Date

May 8, 2026

Last Update Submit

June 4, 2026

Conditions

Keywords

strokestroke sequelaeCognitive Impairement

Outcome Measures

Primary Outcomes (1)

  • Montreal Cognitive Assessment

    To detect mild cognitive impairment and assess for early stages of dementia. This scale utilizes a minimum value of 0 and a maximum value of 30, where higher scores mean a better outcome (a score of 26 or above is considered normal, while a score of 22 suggests mild cognitive impairment.

    4 weeks

Interventions

Combined somatotherapy and occupational therapy delivered during inpatient hospitalization. Somatotherapy consisted of structured sensorimotor and physical therapy targeting body awareness, movement, balance, and coordination. Occupational therapy focused on patient-specific, task-oriented training in activities of daily living (ADLs) such as self-care, functional mobility, and cognitive integration during daily tasks. Patients received 35-minute sessions, 5 days per week for 4 consecutive weeks. Therapy was customized according to individual patient needs and used equipment including adjustable tables, chairs, wheelchairs, and assistive aids (splints, glasses, etc.).

Eligibility Criteria

Age30 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

50 post-stroke patients (30 males and 20 females) who were referred to the Department of Physical Therapy at King Hospital, Swat, Pakistan between 2018 and 2019 for cognitive rehabilitation. Participants were adult stroke patients (approximate mean age around 60 years) with either ischemic or hemorrhagic stroke who received 4 weeks of inpatient combined somatotherapy and occupational therapy.

You may qualify if:

  • Adults aged 30 years and above
  • Diagnosed with ischemic or hemorrhagic stroke (first-ever or recurrent)
  • Referred to physical therapy department for cognitive rehabilitation
  • Received somatotherapy and occupational therapy during hospitalization
  • Able to undergo MoCA (Montreal Cognitive Assessment) testing

You may not qualify if:

  • Severe speech impairment (aphasia) that prevents reliable cognitive testing
  • Significant visual impairment that interferes with MoCA testing
  • Significant hearing impairment that interferes with MoCA testing
  • Inability to participate in therapy sessions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Swat Medical Complex

Swat, Khyber Pakhtunkhwa, 26000, Pakistan

Location

MeSH Terms

Conditions

Cognitive DysfunctionStroke

Interventions

Occupational Therapy

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental DisordersCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

RehabilitationAftercareContinuity of Patient CarePatient CareTherapeutics

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
50 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Prof.

Study Record Dates

First Submitted

May 8, 2026

First Posted

June 9, 2026

Study Start

January 3, 2023

Primary Completion

December 25, 2025

Study Completion

December 25, 2025

Last Updated

June 9, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

ndividual participant data will not be shared publicly. The study is a small retrospective analysis based on hospital medical records. Sharing IPD is not planned due to: Ethical and privacy concerns (patient confidentiality and data protection regulations). The retrospective nature of the study with no prior consent obtained from participants for data sharing. Local institutional policies at King Hospital regarding data sharing.

Locations