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The Effect of Foot Reflexology Massage on Neuropathic Pain

The Effect of Foot Reflexology Massage Applied to Women With Type 2 Diabetes on Neuropathic Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06951412
Enrollment
65
Registered
2025-04-30
Start date
2023-03-01
Completion date
2024-03-15
Last updated
2025-04-30

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

Conditions

Type 2 Diabetes

Keywords

Foot massage, Reflexology, Neuropatic pain, Nursing, neuropathy

Brief summary

This study is conducted to measure the effect of foot reflexology massage on neuropathic pain in diabetic patients.Is reflexology foot massage applied to type 2 diabetic patients effective on neuropathic pain?

Detailed description

Controlling pain in individuals with diabetes; It is important for the individual to relax, increase the quality of life, reduce complications and shorten the duration of hospital stay. For this reason, the importance of neuropathic pain and its treatment is increasing in terms of public health. In this study, the effect of foot reflexology massage applied to women with type 2 diabetes on neuropathic pain was measured.

Interventions

Reflexology Massage

Sponsors

University of Gaziantep
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

experimental and control group

Intervention model description

At this stage, the patients in the intervention group received a foot reflexology massage by the researcher in the podiatry room of the Endocrinology and Metabolic Diseases polyclinic in a quiet and calm environment for 6 weeks, two sessions per week, for a total of 12 sessions and 30-40 minutes (15-20 minutes for each foot). Data collection forms were filled out for the patients in the control group, but no application was made.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Those diagnosed with type 2 diabetes, 2. Being 18 years or older 3. Individuals who do not have any fractures in the extremities, skin diseases, past wound history, open wounds and unilateral or bilateral amputation, tendonitis in the ankle, active foot ulcer and infection. 4. Those who volunteer to participate in the study, 5. Those who do not have problems with verbal communication, 6. Those who have not been diagnosed with any psychiatric disease. 7. Those with neuropathic pain of 12 points and above according to the LANS score 8. Patients receiving duloxetine drug therapy 9. Those who are not pregnant 10. Patients without peripheral artery disease, deep vein thrombosis and gonatosis will be included in the study. -

Exclusion criteria

1. Those who did not agree to participate in the study 2. Those under 18 years of age 3. Individuals with no fractures in the extremities, skin diseases, past wound history, open wounds and unilateral or bilateral amputation, tendonitis in the ankle, active foot ulcers and infections. 4. Those who have problems with verbal communication 5. Those with neuropathic pain below 12 points according to the LANS score 6. Patients receiving treatment other than duloxetine drug therapy 7. Those who are pregnant 8. Those with any psychiatric disorder 9. Patients with peripheral artery disease, deep vein thrombosis and gonatosis will not be included in the study.-

Design outcomes

Primary

MeasureTime frameDescription
pain score6 Weeksvisual analog scale:VAS: It is a scale scored between 0 and 10 points. A score of 0 indicates that the patient has no pain, and a score of 10 indicates that the patient has unbearable pain. The patient gives a score between 0 and 10 depending on the pain condition.

Secondary

MeasureTime frameDescription
Four Question Neuropathic Pain Questionnaire6 weeksThis questionnaire consists of a total of 10 items; 7 items are related to the quality of pain (burning, painful cold, electric shocks) and its relationship with abnormal sensations (tingling, pins and needles, numbness, itching), and 3 items are related to the clinical examination of the painful area (touch hypoesthesia, pricking hypoesthesia, tactile allodynia). Each item is scored 1 if the answer is yes and zero if no, with a minimum of zero and a maximum of 10 points. In this assessment, a score of ≥4 out of 10 is considered neuropathic pain

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026