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Studying the effect of ear acupressure on motor function and quality of life in stroke patients: A double-blind randomized clinical trial

Comparing the effectiveness of ear acupressure with usual care on motor function and quality of life in stroke patients: A randomized, double-blind clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131204015649N6
Enrollment
150
Registered
2026-01-04
Start date
2026-02-20
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

stroke. Brain stem stroke syndrome

Interventions

Intervention 1: Control group: Patients in the control group will undergo a similar protocol using non-magnetic (sham) beads. The inert beads will be placed on sham points (points distant from establi

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Definitive diagnosis of ischemic stroke by a neurologist. Presence of hemiplegia (paralysis of one side of the body). Alertness and ability to communicate and collaborate with the research team. Having a Barthel Index score equal to or less than 60. Being in the early recovery period (from 24 hours to one week after the stroke). Being in stages one to four of the Bronstrom classification for the upper and lower extremities.

Exclusion criteria

Exclusion criteria: Intracranial hemorrhage during the procedure Presence of extreme fatigue or severe infection that makes participation in the study impossible. Concomitant malignant tumors or serious diseases of the heart, liver, kidneys, or other organs. Having physical pain or movement limitations due to other conditions (such as unilateral inattention, severe proprioception disorder, blindness, or limb dislocation). Previous history of using ear acupressure or acupuncture. Inability to understand instructions or complete questionnaires due to severe cognitive or communication impairment (mental state test score less than 23). The patient's personal desire to withdraw from further participation at any stage of the study

Design outcomes

Primary

MeasureTime frame
Change in mean global motor function score. Timepoint: Before the start of the intervention and one month after the end of the intervention period. Method of measurement: Standard Vohl-Meyer Questionnaire.

Secondary

MeasureTime frame
Change in average quality of life score. Timepoint: Before the start of the intervention and one month after the intervention. Method of measurement: Total score of SS-QOL questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Reza Negarandeh

Tehran University of Medical Sciences

negarandeh@gmail.com+98 51 3858 3786

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026