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Reflexology effect on sleep disorders and pain after abdominal surgery

Effect of reflexology on pain and sleep disorder in older women whith abdominal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016010325625N2
Enrollment
80
Registered
2016-01-24
Start date
2016-01-20
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

Condition 1: Sleep disorder. Condition 2: Pain. Disorders of initiating and maintaining sleep [insomnias] Severe abdominal pain (generalized)(localized)(with abdominal rigidity)

Interventions

Reflexology in the morning( one hour after breakfast) and evening (one hour before bedtime) in the second and third day of surgery and for 20 minutes each will be conducted by the researcher. Interven
did not receive special treatment than the routine care of surgery.
intervention group
Reflexology in the morning( one hour after breakfast) and evening (one hour before bedtime) in the second and third day of surgery and for 20 minutes each will be conducted by the researcher.
The control group

Sponsors

Vice Chancellor of Research- Iran University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for the study; Operation of the surgical incision in the abdomen, according to the length of time of operation, the point 5 of the tool above the PSQI, no disturbance or deformation of the foot (corn, burning feet, amputations and skin diseases), The lack of a history of drug use or psychiatric disorders, absence of diabetes, lack of severe visual-auditory disorders, addiction to alcohol and drugs, having a fracture, graft and wound infections , Mini-Mental State Examination scores Persian versions 7 and above, the ability to self-report pain Exclusion criteria of the study; Lack of cooperation or death of the elderly, less than two days of hospital discharge after surgery, not wanting to continue to participate in the study, any risk of malignancy associated with the surgery, the patient needs to be hospitalized in intensive care unit.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Improving in sleep quality. Timepoint: Half an hour before the intervention and the fourth day of surgery. Method of measurement: Pittsburgh Sleep Quality Index.;Pain relief. Timepoint: Half an hour before the intervention and the fourth day of surgery. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
-. Timepoint: -. Method of measurement: -.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzade khriri

Faculty of Nursing and Midwifery, Iran University of Medical Science

kheiri.a@iums.ac.ir+98 51 4324 5417

Outcome results

None listed

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