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Investigating the Effects of Acupressure on Sleep Quality, Anxiety, and Physiological Indicators in Patients with Heart Failure

Investigating the Effects of Acupressure on Sleep Quality, Anxiety, and Physiological Indicators in Patients with Heart Failure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190524043687N6
Enrollment
76
Registered
2025-12-19
Start date
2025-12-31
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

Heart failure. Heart failure

Interventions

Intervention 1: Intervention Group: Patients with heart failure in the intervention group will first complete questionnaires assessing sleep quality and anxiety, and their physiological parameters, in

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Willingness to Participate in the Study Signing of Informed Consent Form Ability to speak and understand the Persian language Diagnosed heart failure (EF < 40%), as confirmed by the treating physician

Exclusion criteria

Exclusion criteria: Presence of conditions such as intellectual disability, mental or behavioral disorders, hearing impairment, or speech disorders Presence of a previously diagnosed psychiatric disorder and/or sleep disorder Use of complementary therapies prior to the study Presence of addiction to alcohol, illicit drugs, or sedative medications Use of sedative or anti-anxiety medications within the past 24 hours Presence of any contraindication at the pressure application site (e.g., wounds, skin diseases, etc.)

Design outcomes

Primary

MeasureTime frame
Sleep Quality. Timepoint: Before the start of the study and on the second, third, and fourth days of hospitalization. Method of measurement: Pittsburgh Sleep Quality Index (PSQI).;Anxiety. Timepoint: Spielberger Anxiety Questionnaire. Method of measurement: Before, immediately after, and 30 minutes after the daily intervention.;Arterial oxygen saturation. Timepoint: Before, immediately after, and 30 minutes after the daily intervention. Method of measurement: Pulse oximetry.;Systolic blood pressure. Timepoint: Before, immediately after, and 30 minutes after the intervention. Method of measurement: Digital sphygmomanometer.;Diastolic blood pressure. Timepoint: Before, immediately after, and 30 minutes after the intervention. Method of measurement: Digital sphygmomanometer.;Heart rate. Timepoint: Before, immediately after, and 30 minutes after the intervention. Method of measurement: Pulse oximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Afshari

Hamedan University of Medical Sciences

afshari777@gmail.com+98 81 3838 0447

Outcome results

None listed

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