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Manual Lymphatic Drainage for Pain, Muscle Strength, and Sensation

Effect of Manual Lymphatic Drainage on Pressure Pain Threshold, Pain Tolerance, Grip and Pinch Strength, and Two-point Discrimination

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06139445
Enrollment
82
Registered
2023-11-18
Start date
2023-11-08
Completion date
2023-11-30
Last updated
2024-01-29

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

Conditions

Manual Lymphatic Drainage Effects

Keywords

Manual lymphatic drainage, pain threshold, pain tolerance, two-point discrimination, muscle strength

Brief summary

To evaluate the acute effect of MLD on pressure pain threshold (PPT), pain tolerance, tactile sensation, and muscle strength in healthy young adults. healthy young adults were included in the study. Before and after MLD and plasebo touchs, the same physiotherapist performed PPT and pain tolerance measurements, muscle strength measurements with a hand dynamometer (Jamar®) and pinchmeter (Baseline®), and two-point discrimination (2PD) evaluation with an esthesiometer.

Interventions

OTHERManual Lymphatic Drainage

Manual lymphatic drainage (MLD), one of the components of complex decongestive physiotherapy, is a gentle massage technique with proven positive effects on lymphatic circulation. MLD can be applied to different parts of the body (e.g., arms, legs, neck, abdomen, and trunk), with a different technique for each region (stationary circle, scoop, pump, and rotary)

random superficial touches not involved in any manual technique

Sponsors

Selcuk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Being aged 18-30 years * Volunteering to participate in the study

Exclusion criteria

* Having any skin disease * Having a history of neurological and/or orthopedic disease * Having a significant scar or burn tissue in the upper extremity * Having any condition that would prevent communication

Design outcomes

Primary

MeasureTime frameDescription
pressure pain threshold (PPT)5 minutesPPT measurements will be performed using a 1-cm2 surface algometer.The algometer will be positioned vertically and placed on the thenar, hypothenar, mid-ulnar, and biceps regions using the marked points. Measurements will be repeated three times. The average of these three measurements will be used for analysis.
pain tolerance5 minutespain tolerance measurements will be performed using a 1-cm2 surface algometer.The algometer will be positioned vertically and placed on the thenar, hypothenar, mid-ulnar, and biceps regions using the marked points.The highest tolerable pressure will be used in the measurement and it will be recorded.
Evaluation of Hand Grip Strength5 minutesThe Jamar will be used to measure hand grip strength.Three measurements will be made at one-minute intervals, and the average values will be recorded
Evaluation Finger Pinch Strength5 minutesA pinchmeter (Baseline®) will be used to measure finger pinch strength. Three measurements will be made at one-minute intervals, and the average values will be recorded
Two-point discrimination (2PD)10 minutesThis evaluation will be performed using an esthesiometer with the participants in the sitting position with their eyes closed. Evaluation will be made from the biceps medial to the elbow. The contact time of the two-point stimulation will be adjusted to be approximately 1-2 seconds, and approximately 3-5 seconds will be waited between each stimulation. The shortest distance felt between two points provided the static 2PD value

Countries

Turkey (Türkiye)

Outcome results

None listed

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