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Effect of acupressure on constipation of hemodialysis patients

Compare of acupressure and pressure on false points on constipation of patients with chronic renal failure undergoing hemodialysis in control and intervention groups

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015043022027N1
Enrollment
60
Registered
2015-07-28
Start date
2015-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic Renal failure. Chronic kidney disease, stage 5

Interventions

Intervention 1: Control group: Doing acupressure on false points. Intervention 2: Intervention group: Doing acupressure 3 times and each times for 1 minute in points of acupressure: three knuckle from
Treatment - Other
Control group: Doing acupressure on false points
Intervention group: Doing acupressure 3 times and each times for 1 minute in points of acupressure: three knuckle from midline of abdomen in both sides of umbilicus, between the index finger and thumb

Sponsors

Vice Chancellor for research of Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Having constipation based on Rom 3 criteria (having 2 criterion from 6 criterion of constipation); having at least 6 months of hemodialysis; having dossier in dialysis unit; having hemodialysis 3 times and every times 4 hours in weeks; having full consciousness and ability of hearing and speaking; not having skin disease, progressive heart failure or stroke based on claim of patients; not having amputation or an ulcer at the site of acupressure; not using from laxatives in recently month; not having digestive disorders such as irritable bowel syndromes based on claim of patient, history and physical examination. Exclusion Criteria: Disrupting or failure to completing the study because of transition to acute care unit; death, traveling or having transplantation surgery; stressful life event such as death of relatives; unwillingness to continue the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Daily defecation. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Daily number of defecation.;Quality of stool. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: compare of shape of stool with pictures of stool (based on Bristol criterion).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Mojalli

Gonabad University of Medical Sciences

Mojalli.m@gmu.ac.ir+98 51 5722 5027

Outcome results

None listed

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