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Can Acupuncture Benefit Surgical Patients With Haemorrhagic Stroke?

Can Acupuncture Benefit Surgical Patients With Haemorrhagic Stroke?

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01037894
Enrollment
55
Registered
2009-12-23
Start date
2009-01-31
Completion date
2012-09-30
Last updated
2013-01-14

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

Conditions

Stroke

Keywords

Acupuncture,Intracerebral hemorrhage, Stroke

Brief summary

The purpose is to establish whether acupuncture in addition to conventional rehabilitation programme can improve the functional outcome and quality of life of surgical patients with haemorrhagic stroke, as compared to conventional rehabilitation programme alone.

Detailed description

The investigators aim to recruit 60 patients over a 30 month period. Each patient will have six week of acupuncture treatment (either early within the first six week, or delayed after the first six week of observation and assessment of primary outcome). Primary outcome measures: Clinical outcome at the end of week 6 acupuncture treatment: Glasgow Outcome Score extended. Secondary outcome measures: Modified Rankin Score, Functional Independence Measure (FIM) score, Modified Aschoff Score, Neurocognitive State Examination (NCSE) score, Barthel index, Modified Rivermead Mobility Index (MRMI), Modified Functional Ambulation Category (MFAC) and motor scores of upper limb and lower limb with Fugl-Meyer Scale at the end of week six acupuncture treatment.

Interventions

PROCEDUREAcupuncture

Acupuncture from physiotherapist (with accredited training in acupuncture) in Shatin Hospital, three sessions per week for six weeks, and each session 30 minutes.

PROCEDUREConventional rehabilitation

In-patient physiotherapy, occupational therapy and speech therapy.

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Patient inclusion Criteria: 1. Patients after acute hemorrhagic stroke; 2. Within the first month after acute presentation; 3. Premorbid mobility level: Independent Indoor or Outdoor Walker; 4. Co-operative and willing to comply with the rehabilitation program; Patient

Exclusion criteria

1. Cardiac Pacemaker; 2. Patient who is apprehensive to acupuncture; 3. Clotting abnormality; 4. Poor local skin conditions.

Design outcomes

Primary

MeasureTime frame
Glasgow Outcome Scale ExtendedSix week

Secondary

MeasureTime frame
Modified Aschoff ScoreSix week
Neurocognitive State Examination(NCSE)scoreSix week
Motor scores of upper limb and lower limb with Fugl-Meyer Scalesix week
Functional Independence Measure (FIM) scoreSix week
Modified Rivermead Mobility Index (MRMI)Six week
Barthel IndexSix week
Modified Rankin ScaleSix week
Modified Functional Ambulation Category (MFAC)Six week

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026