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Effects of Massage Therapy on Peripheral Neuropathy and Quality of Life

F

Fatma Arikan

Status

Completed

Conditions

Chemotherapy-induced Peripheral Neuropathy

Treatments

Behavioral: Massage therapy group

Study type

Interventional

Funder types

Other

Identifiers

NCT05433246
2011/211

Details and patient eligibility

About

The aim of this randomized controlled experimental study was to determine the effect of massage applied to colorectal cancer patients receiving chemotherapy on peripheral neuropathy and quality of life.

Full description

The aim of this randomized controlled experimental study was to determine the effect of massage applied to colorectal cancer patients receiving chemotherapy on peripheral neuropathy and quality of life.Investigation was carried out between February 2012- May 2013 with 52 patients meeting study criteria and receiving chemotherapy in Akdeniz University outpatient chemotherapy unit (28 study group, 24 control).

Massage therapy group:The experimental group patients were given a series of effleurage, petrissage and surface fraction types of classical massage on local parts of they're body-below, elbow-frontal arm-hand (20 minutes) and below knee-leg (lower part)-foot (20 minutes) two days of treatment of 16 times total.The patients in the massage group received 16 sessions of classical massage performed by the research nurse, who had classical massage training and certification.Baseline, patient characteristics , peripheral neuropathy symptoms, neuropathic pain, cancer and chemotherapy-related symptoms, and quality of life were completed. Peripheral neuropathy symptoms, cancer, and chemotherapy-related symptoms were assessed at each cycle (2th, 4th, 6th, 8th,10th,12th,14th, 16th. week- (two-week intervals)). Neuropathic pain and quality of life were measured at 4, 10, and 16 weeks. At week 16 (2 weeks after the intervention), the grade of peripheral sensory neuropathy was determined.

Control Group: The patients received routine care. Baseline, patient characteristics , peripheral neuropathy symptoms, neuropathic pain, cancer and chemotherapy-related symptoms, and quality of life were completed. Peripheral neuropathy symptoms, cancer, and chemotherapy-related symptoms were assessed at each cycle (2th, 4th, 6th, 8th,10th,12th,14th, 16th. week (two-week intervals)). Neuropathic pain and quality of life were measured at 4, 10, and 16 weeks. At week 16 (2 weeks after the intervention), the grade of peripheral sensory neuropathy was determined.

Enrollment

52 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • over 18 years old
  • have a diagnosis of colorectal cancer
  • receiving FOLFOX-4 chemotherapy protocol
  • to receive a maximum of 4 cycles of FOLFOX-4 chemotherapy
  • platelet values over -100.000/mm3
  • no obstacle to massage application

Exclusion criteria

  • previously been diagnosed with polyneuropathy,
  • has been diagnosed with diabetes,
  • is addicted to alcohol,
  • has been amputated at the extremities,
  • has a skin infection and skin integrity disorder,
  • has megaloblastic anemia, uses anticoagulants,
  • takes drugs that hide or affect neuropathy findings
  • has had massage therapy within the last month.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

52 participants in 2 patient groups

Control Group
No Intervention group
Description:
The patients received routine care.
Massage therapy group
Experimental group
Description:
The patients in the massage group were given classical massage for 2 consecutive days in each chemotherapy cycle (with an interval of two weeks). Massage therapy was performed with a classical massage technique using effleurage, petrissage, and superficial friction techniques for a total of 40 minutes on the areas below the elbow-forearm-hand (20 minutes), and below the knee-lower leg-foot (20 minutes). The patients in the massage group received 16 sessions of classical massage performed by the research nurse, who had classical massage training and certification.
Treatment:
Behavioral: Massage therapy group

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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