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Effect of the massage therapy on the patients with acute blood cancer

Effect of the Slow Stroke Back Massage on the pain and fatigue severity in the patients with acute leukemia undergoing chemotherapy.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015030221307N1
Enrollment
Unknown
Registered
2015-05-13
Start date
2015-04-19
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

Acute leukemia. Acute lymphoblastic leukaemia [ALL], Acute myeloblastic leukaemia [AML]

Interventions

Both groups will receive the routine cares. The intervention group will be treated with slow stroke back massage. 1- The patient sits on a chair and leaned his head on the pillow, 2 - The small rotati
Both groups will receive the routine cares. The intervention group will be treated with slow stroke back massage. 1- The patient sits on a chair and leaned his head on the pillow, 2 - The small rotat

Sponsors

Ahvaz Jundishapur University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ages ranging from 18 to 50 years; pain and fatigue severity 3 or more (on the basis of numeric rating scale); no sign of clear and identified pain or fatigue disorders which are recorded in patients' files (pains from lumbar disc, spinal injuries, fractures, etc. and fatigue from Thalassemia, Sickle cell anemia, etc.); not having any background diseases (such as diabetes, peripheral nerves disease); the patients should have been under chemotherapy. Exclusion criteria: absence in two sessions of massage therapy; discharge or death of the patient; and the patient's unwillingness to continue to participate in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: Before intervention, at the end of each week, after intervention. Method of measurement: Numeric rating scale (NRS).;Fatigue severity. Timepoint: Before intervention, at the end of each week, after intervention. Method of measurement: Numeric rating scale (NRS).

Secondary

MeasureTime frame
Nausea severity. Timepoint: Before intervention, at the end of each week, after intervention. Method of measurement: Numeric rating scale (NRS).;Quality of life. Timepoint: Before and after of intervention. Method of measurement: Short-Form 36 Health Survey (SF-36).;Sleep quality. Timepoint: Before and after of intervention. Method of measurement: Pittsburgh Sleep Quality Index (PSQI).;Mood disturbances. Timepoint: Before and after of intervention. Method of measurement: Beck Depression questionnaire and Spielberg Anxiety questionnaire.;Sleep disturbance severity. Timepoint: Before intervention, at the end of each week, after intervention. Method of measurement: Numeric rating scale (NRS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahram Baraz

Ahvaz Jundishapur University of Medical Sciences

shahrambaraz@yahoo.com+98 61 3373 8333

Outcome results

None listed

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