Skip to content

The effect of acupressure training to family caregiver on dyspnea and subjective wellbeing in hospitalized patients with chronic heart failure in cardiac care units

The effect of acupressure training to family caregiver on dyspnea and subjective wellbeing in hospitalized patients with chronic heart failure in cardiac care units

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110906007494N38
Enrollment
50
Registered
2021-07-22
Start date
2021-07-22
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Dyspnea. Shortness of breath

Interventions

Intervention 1: Intervention group: in acupressure group, in addition to drug treatment, 5 points BL13, LU9, LU1, BL15, P6 will be pressed symmetrically and bilaterally. Acupressure will be performed

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Complaints of shortness of breath Six months have passed since the definitive diagnosis of the disease Age older than 18 years old Heart failure stage 2 to 4 Speaking and understanding Persian language Do not take drugs and sedatives No education in the field of medicine or traditional medicine Absence of severe diabetic neuropathy No history of neurological disease, asthma, COPD, cancer and other respiratory diseases diagnosed by a doctor Not being blind and deaf Possibility to contact the patient or one of his family members No pregnancy No history of using acupressure No wounds or scratches or deformities

Exclusion criteria

Exclusion criteria: Reluctance to continue participating in the study for any reason Incidence of complications and physical and mental disorders during the study Loss of the ability to execute the plan due to new physical problems Failure to intervene in more than a quarter of the designated days (7 days)

Design outcomes

Primary

MeasureTime frame
Dyspnea. Timepoint: At the beginning of the study, after 2 weeks and after 4 weeks. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Subjective wellbeing. Timepoint: At the beginning of the study, after 2 weeks and after 4 weeks. Method of measurement: 5- Item World Health Organization Well-Being Index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Bagheri Nesami

Mazandaran University of Medical Sciences

mbagheri@mazums.ac.ir+98 11 3336 7551

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026