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The effect of acupressure on the thirst of hemodialysis patients

The effect of acupressure on the thirst of hemodialysis patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250930067439N1
Enrollment
90
Registered
2025-10-17
Start date
2025-10-23
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Chronic kidney disease. Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or histology), albuminuria above normal limits, urinary sedime

Interventions

Intervention 1: Intervention group: participants who have acupressure applied to the LU-7, LI-4, KI-2, LR-2 points. Intervention 2: Control group: Participants in the sham group will have acupressure

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Participants aged between 18 and 65 years Written informed consent obtained prior to enrollment in the study Patients undergoing maintenance hemodialysis who have experienced symptoms of thirst during the past month Regular hemodialysis schedule, defined as three sessions per week No previous exposure to acupressure or other complementary therapies such as acupuncture Absence of any acute or chronic medical condition that may contraindicate the application of acupressure (e.g., advanced heart failure, soft tissue or vascular disorders of the limbs, or sensory–neurological impairments in the target areas) No active dermatological issues at the intended pressure sites, including wounds, inflammation, or rash No history of acupressure or acupuncture within the preceding three months Not currently taking medications known to affect salivation or thirst (e.g., tricyclic antidepressants, anticholinergics, antihistamines, or beta-blockers) No recent history of surgery or infection in the limbs Intact cognitive function, full consciousness, and the ability to understand and follow verbal instructions

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Thirst. Timepoint: Before the start of the intervention, the participants’ level of thirst will be assessed using two instruments: the Visual Analog Scale (VAS) and the Dialysis Thirst Inventory (DTI).In this study, acupressure will be applied in both the intervention and sham groups once daily (either in the morning or in the evening) for a duration of 2.5 minutes per point, over a period of four consecutive weeks.The researcher will evaluate the participants’ thirst level at the end of each dialysis session using the VAS, and at the end of each week using the DTI, in both the intervention and sham groups. Method of measurement: using two instruments: the Visual Analog Scale and the Dialysis Thirst Inventory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Bagheri

Mashhad University of Medical Sciences

BagheriM@mums.ac.ir+98 51 3884 6730

Outcome results

None listed

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