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Acupuncture and Computer-based Training to Improve Attention Deficits in Patients After Stroke

Evaluation of Acupuncture and Attention Training Effects on Patients After Stroke: a Study Protocol of an International Multicentre Study Using a Randomized Single Blinded Three-group Design

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02324959
Acronym
ACoTrain
Enrollment
60
Registered
2014-12-24
Start date
2014-11-30
Completion date
2016-01-31
Last updated
2014-12-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Brief summary

The purpose of this study is to determine whether acupuncture and computer-based attention training can be combined for more effective post-stroke attentional deficits.

Interventions

DEVICERehaCom

The computer-based neurorehabilitation program is intended for patients with acquired cognitive deficits after brain damage, e.g. after stroke. The RehaCom software has five different therapeutic groups aimed at restoration of attention, memory, executive functions, and visual field, respectively. Each group has one to four different modules to choose from for each therapy session. Only attention will be trained in this study.

DEVICEAcupuncture

The affected meridian group is treated by needling on Baihui (GV20\|DU20) and Shenting (GV24\|DU24) - both acupoints of the Governor Vessel. Baihui is 5 cun (1cun=3.33 cm) superior to the anterior hairline on the anterior median line (midpoint of the connecting line between the auricular apices).

Sponsors

Reha Rheinfelden
CollaboratorOTHER
m&i-Fachklinik Herzogenaurach
CollaboratorUNKNOWN
Fujian University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Admitted to inpatient stroke rehabilitation within six months after first-ever stroke * Mild cognitive impairments (attention performance TAP \> 1 standard deviation below mean age-matched norm in at least one subtest). * Conscious, stable physical condition and signed informed consent of patient.

Exclusion criteria

* Severe visual and/or hearing problems * Inability to follow instructions (MoCA) * Disorders of speech and instruction comprehension (tested with a modified token-test) * Severe visual and/or hearing problems * Pre-existing mental disorders - Pregnancy

Design outcomes

Primary

MeasureTime frame
Change from Baseline in attention performance at 4 weeks (Test Battery for Attention Performance (TAP))Pretest (day 1), Posttest (4 weeks)

Secondary

MeasureTime frame
Change from Baseline in number of errors for the Test des Deux Barrage (T2B) at four weeks.Pretest (day 1), Posttest (4 weeks)
Change from Baseline in number of omissions for the Test des Deux Barrage (T2B) at four weeks.Pretest (day 1), Posttest (4 weeks)
Change from Baseline in time needed for Trail Making Test (TMT A/-B) at four weeks.Pretest (day 1), Posttest (4 weeks)
Change from baseline in total score of Extended Barthel Index (EBI) at four weeks.Pretest (day 1), Posttest (4 weeks)
Change from baseline score of EuroQol quality of life questionnaire (EQ-5D 3L) at four weeks.Pretest (day 1), Posttest (4 weeks)
National Institute of Health Stroke Scale (NIH-SS)Pretest (day 1)

Countries

China, Germany, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026