Skip to content

The effect of foot reflexology on fatigue, pain and physiological parameters in patients after coronary angiography

The effect of foot reflexology on fatigue, pain and physiological parameters in patients after coronary angiography

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015072223286N1
Enrollment
35
Registered
2016-04-08
Start date
2016-03-20
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: Fatigue. Condition 2: Pain. Condition 3: Angiography. Other specified neurotic disorders Acute pain Abnormal findings on diagnostic imaging of heart and coronary circulation

Interventions

Intervention 1: In reflexology group, massage is done by researcher and man collaborator( for male patients ) )for 10 minutes(5 minutes per foot). The sequence are used of relaxation and specific area
In reflexology group, massage is done by researcher and man collaborator( for male patients ) )for 10 minutes(5 minutes per foot). The sequence are used of relaxation and specific areas of the heart.
In the control group intervention will not occur, except routine care and vital signs measurement.fatique ,pain and physiologic parameters Questionnaire recorded by collaborator and with presence of r

Sponsors

Vice Chancellor for Research Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: willingness to participate in research ; non-emergency angiography ; The age range of eighteen to seventy-five years ; No disturbance of consciousness ; Lack of vascular injuries of the lower limbs and sensory-motor disorders of the feet (especially Diabetic Foot) ; The absence of abnormalities such as corns, burns, amputations and skin disorders in the legs ; lack of inter-vertebral disc herniation, low back pain and back pain Exclusion criteria: Failure to consent to continued participation ; Death participants ; hemodynamic instability (dysrhythmia, respiratory disorders, and severe changes in blood pressure requiring emergency interventions ; bleeding after angiography

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fatigue. Timepoint: Baseline and 2, 4 and 6 hours after intervention. Method of measurement: Visual Analoge Scale for Fatigue.;Pain. Timepoint: Baseline and 2, 4 and 6 hours after intervention. Method of measurement: Visual Analoge Scale for Pain.;Blood pressure. Timepoint: Baseline and 2, 4 and 6 hours after intervention. Method of measurement: Tytan Blood Pressure Devices.;Pulse. Timepoint: Baseline and 2, 4 and 6 hours after intervention. Method of measurement: According to minutes using the standard clock.;Breathing. Timepoint: Baseline and 2, 4 and 6 hours after intervention. Method of measurement: According to minutes using the standard clock.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Shokatiasl

Faculty of Nursing and Midwifery? Tehran University of Medical Sciences

a-shokati@razi.tums.ac.ir; shokati16@yahoo.com+98 21 4432 3872

Outcome results

None listed

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