NCT01374152

Brief Summary

The cognitive sensory motor training therapy (Perfetti's technique) might be more effectiveness than conventional occupational therapy on upper extremity function recovery after acute stroke patients.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
40

participants targeted

Target at below P25 for phase_3 stroke

Timeline
Completed

Started Jul 2008

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2008

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2011

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2011

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

June 14, 2011

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 15, 2011

Completed
Last Updated

July 17, 2012

Status Verified

July 1, 2012

Enrollment Period

2.8 years

First QC Date

June 14, 2011

Last Update Submit

July 15, 2012

Conditions

Stroke

Keywords

strokeupper extremityrehabilitationperfetti

Outcome Measures

Primary Outcomes (1)

  • Action research arm test

    The Action research arm test used for assess the impairment of upper limb function. ARAT has ordinal 4-point scale (0-3) in 19 items. Totally 57 scores.

    4 weeks

Secondary Outcomes (2)

  • Box and block test

    4 weeks.

  • Extended Barthel Index

    4 weeks.

Study Arms (2)

Perfetti

EXPERIMENTAL

Cognitive sensory motor training method for upper extremities rehabilitation every working day, totally training not less than 600 minutes within 4 weeks.

Other: cognitive sensory motor training therapy

conventional rehabilitation

NO INTERVENTION

conventional occupational therapy method for upper extremities rehabilitation every working day, totally training not less than 600 minutes within 4 weeks.

Interventions

cognitive sensory motor training therapyOTHER

training method that emphasis on cognition/ sensation/ and motor movement together train every working day 45 minutes per day for 4 weeks.

Also known as: Perfetti, Cognitive sensory motor training, Stroke, Upper extremity
Perfetti

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • First ever stroke
  • Impaired upper extremity function
  • Given signed inform consent

You may not qualify if:

  • Unstable medical condition
  • Any upper extremity functional impairment prior to stroke
  • Can not adequately cooperate in training
  • Severe communication problems
  • Severe cognitive - perceptual deficits
  • Fixed contracture more than 30 degree in every upper extremity joint

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Prasat neurological institute

Bangkok, Bangkok, 10400, Thailand

Location

Related Publications (3)

  • Wongphaet P, Butrach W, Sangkrai S, Jitpraphai C. Improved function of hemiplegic upper extremity after cognitive sensory motor training therapy in chronic stroke patients: preliminary report of a case series. J Med Assoc Thai. 2003 Jun;86(6):579-84.

    PMID: 12924807BACKGROUND

  • Duncan PW, Goldstein LB, Horner RD, Landsman PB, Samsa GP, Matchar DB. Similar motor recovery of upper and lower extremities after stroke. Stroke. 1994 Jun;25(6):1181-8. doi: 10.1161/01.str.25.6.1181.

    PMID: 8202977BACKGROUND

  • Lyle RC. A performance test for assessment of upper limb function in physical rehabilitation treatment and research. Int J Rehabil Res. 1981;4(4):483-92. doi: 10.1097/00004356-198112000-00001. No abstract available.

    PMID: 7333761BACKGROUND

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Ratanapat Chanubol, MD.

    Prasat Neurological Institute

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr.

Study Record Dates

First Submitted

June 14, 2011

First Posted

June 15, 2011

Study Start

July 1, 2008

Primary Completion

May 1, 2011

Study Completion

June 1, 2011

Last Updated

July 17, 2012

Record last verified: 2012-07

Locations

TH(1)