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To investigate the effect of Solar plexus reflexology of sole of the foot on pain, anxiety and physiological Indicators caused by bone marrow aspiration (BMA) in patients with leukemia

To investigate the effect of Solar plexus reflexology of sole of the foot on pain, anxiety and physiological Indicators caused by bone marrow aspiration (BMA) in patients with leukemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190524043687N2
Enrollment
70
Registered
2021-08-29
Start date
2021-09-21
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Condition 1: Acute lymphoblastic leukemia. Condition 2: Pain. Condition 3: Anxiety. Condition 4: Acute myeloblastic leukemia. Acute lymphoblastic leukemia [ALL] Pain, unspecified Generalized anxiety disorder Acute myeloblastic leukemia

Interventions

Intervention 1: Intervention group: Performing massage intervention in the reflection points of the sole of the foot. For this purpose, the researcher will start the massage intervention 10 minutes af

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Catching leukemia (lymphoblastic or Myeloblastic) The age range of 18 to 60 Signature of informed consent form do bone marrow aspiration for the first time Have literacy to complete the questionnaire

Exclusion criteria

Exclusion criteria: Previous experience or awareness of the impact of acupressure Lack of full consciousness, having mental, visual and auditory disorders History of taking anti-anxiety and sedative drugs one week before participating in the study (based on the contents of the file) Drug addiction Existence of an obstacle at the site of pressure (wounds, skin diseases, etc) Existence of sensory and motor disorders in the legs and minimal ability to walk on the legs (peripheral neuropathy or vascular problems in the lower extremities)

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before intervention, immediately before intervention and after intervention. Method of measurement: Numeric pain rating scale (NRS).;Heart beat. Timepoint: 5 minutes before the intervention, immediately before the intervention, immediately after the intervention, 5 minutes after the intervention. Method of measurement: Number of beats per minute - pulse oximeter.;Arterial blood oxygen saturation (SPO2). Timepoint: 5 minutes before the intervention, immediately before the intervention, immediately after the intervention, 5 minutes after the intervention. Method of measurement: Percentage - pulse oximeter.;Respiratory rate. Timepoint: 5 minutes before the intervention, immediately before the intervention, immediately after the intervention, 5 minutes after the intervention. Method of measurement: Count per minute - count breathing by observation.;Anxiety. Timepoint: Before intervention, immediately before intervention and after intervention. Method of measurement: The State-Trait Anxiety Inventory -Spielberger.;Blood pressure. Timepoint: 5 minutes before the intervention, immediately before the intervention, immediately after the intervention, 5 minutes after the intervention. Method of measurement: By sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Safdari

Arak University of Medical Sciences

asafdari.nu@gmail.com+98 86 3417 3505

Outcome results

None listed

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