ClinicalTrials.gg
RecruitingNCT07919574Updated Nov 5, 2026

Effectiveness of Kinesio Taping as an Adjunct to Conservative Treatment in Women With Lipedema

An interventional study of Kinesio Taping and Standard Conservative Treatment in Lipedema, sponsored by Hatice Zehra FERHATLAR. Recruiting at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-11-05.

Sponsored by Hatice Zehra FERHATLAR · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Updated Nov 5, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
Female
01

Study summary

This prospective, randomized controlled trial aims to evaluate the effectiveness of kinesio taping as an adjunct to standard conservative treatment in women with stage II lower-extremity lipedema.

A total of 30 women will be randomly assigned to two groups: a control group receiving standard conservative treatment and an intervention group receiving kinesio taping in addition to standard conservative treatment. Both groups will receive patient education, physical activity recommendations, and a standardized home exercise program. The intervention group will additionally receive bilateral lower-extremity kinesio taping twice weekly for six weeks.

Participants will be assessed at baseline, week 6 (end of treatment), and week 10 (four-week follow-up). The primary outcome will be the change in pain intensity measured using the Visual Analog Scale (VAS) at week 6. Secondary outcomes will include lower-extremity functional status (LEFS), quality of life (EQ-5D-3L), walking performance (4-meter walk test), lower-extremity circumference measurements, and pressure pain threshold assessed using an algometer.

The study aims to determine whether adding kinesio taping to standard conservative treatment provides additional clinical benefits in women with lipedema.

02

Conditions studied

  • Lipedema

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Keywords

  • Kinesio Taping
  • Conservative Treatment
  • Lower Extremity Function
  • pain
  • Walking Performance
03

In context

Lipedema

85 studies on the registry are indexed under Lipedema; 32 are open to participants now.

This study's planned enrollment of 30 is below the median of 35 across 42 interventional studies indexed under Lipedema.

Browse Lipedema studies →

Lead sponsor

Hatice Zehra FERHATLAR is the lead sponsor of 4 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

**Inclusion Criteria:**

  • Female participants aged 18-65 years.
  • Clinical diagnosis of stage II bilateral lower-extremity lipedema.
  • Ability to walk independently.
  • Ability and willingness to comply with the treatment and assessment schedule throughout the study.
  • Provision of written .

**Exclusion Criteria:**

  • Presence of primary or secondary lymphedema or lipolymphedema.
  • Pregnancy or breastfeeding.
  • Active infection, cellulitis, open wounds, or active dermatological disease in the areas where kinesio taping will be applied.
  • Known allergy or to kinesio tape or its adhesive components.
  • Active deep vein thrombosis or thromboembolic disease.
  • Severe neurological, rheumatological, or orthopedic disorders that may significantly affect lower-extremity function or walking performance.
  • Severe cardiac, renal, or hepatic failure.
  • Lipedema-related surgery or liposuction within the previous three months.
  • Concurrent participation in another intensive physical therapy or manual lymphatic drainage program that may affect study outcomes.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Conservative Treatment + Kinesio Taping

    Procedure: Kinesio Taping · Behavioral: Standard Conservative Treatment

  • Active comparator
    Conservative Treatment Alone

    Behavioral: Standard Conservative Treatment

Interventions

  • ProcedureKinesio Taping

    Kinesio taping will be applied bilaterally to the lower extremities of participants in the experimental group twice weekly for six weeks, for a total of 12 applications. Kinesio taping will be administered in addition to standard conservative treatment.

  • BehavioralStandard Conservative Treatment

    Standard conservative treatment will consist of patient education regarding lipedema and symptom management, physical activity recommendations, and a standardized lower-extremity home exercise program. This treatment will be provided to participants in both groups during the six-week intervention period.

06

What researchers measure

Primary outcomes

  1. Change in Pain Intensity Measured by the Visual Analog Scale (VAS)

    Time frame: Baseline (week 0), week 6, and week 10

Secondary outcomes

  1. Change in Lower Extremity Functional Scale (LEFS) Score

    Time frame: Baseline (week 0), week 6, and week 10

  2. Change in Health-Related Quality of Life Measured by EQ-5D-3L

    Time frame: Baseline (week 0), week 6, and week 10

  3. Change in Walking Performance Assessed by the 4-Meter Walk Test

    Time frame: Baseline (week 0), week 6, and week 10

  4. Change in Lower Extremity Circumference Measurements

    Time frame: Baseline (week 0), week 6, and week 10

  5. Change in Pressure Pain Threshold (PPT) Measured by Algometry

    Time frame: Baseline (week 0), week 6, and week 10

07

Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Michelini S, Musa F, Vetrano M, Santoboni F, Nusca SM, Latini E, Trischitta D, Michelini S, Iosa M, Vulpiani MC. Defocused and Radial Shock Wave Therapy, Mesotherapy, and Kinesio Taping Effects in Patients with Lipedema: A Pilot Study. Lymphology. 2023;56(1):13-26. PubMed 38019876 ↗
  • Rio-Gonzalez A, Delgado-Perez E, Garcia-Garcia E, Gonzalez-Fernandez L, Garcia-Isidoro S, Cerezo-Tellez E. Physiotherapy Intervention in the Immediate Postoperative Phase of Lipedema Surgery-Observational Study. J Clin Med. 2025 Mar 21;14(7):2137. doi: 10.3390/jcm14072137. PubMed 40217588 ↗
  • Fetzer A. Specialist approaches to managing lipoedema. Br J Community Nurs. 2016 Apr;Suppl:S30-5. doi: 10.12968/bjcn.2016.21.Sup4.S30. PubMed 27046426 ↗

Individual participant data

Plan to share: No

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2026 (actual). Primary completion is estimated for Jan 2027, 4 months after the start.

Of 29 interventional studies with no phase under Lipedema, half reached primary completion within 15 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 31. This study's planned 4 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 30, 2026
First posted
Nov 5, 2026
StartActual
Aug 31, 2026
Primary completionEst.
Jan 15, 2027
CompletionEst.
Jan 15, 2027
Last update
Nov 5, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 5, 2026
Show all 1 update
  1. Nov 5, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07919574
Lead sponsor
Hatice Zehra FERHATLAR
Responsible party
Hatice Zehra FERHATLAR (Physical Medicine and Rehabilitation Specialist, Kanuni Sultan Suleyman Training and Research Hospital) — Sponsor-investigator
First posted
Nov 5, 2026
Start date
Aug 31, 2026
Primary completion
Jan 15, 2027 (estimated)
Completion
Jan 15, 2027 (estimated)
Last update
Nov 5, 2026

Study contacts

Hatice Zehra FERHATLAR
Contact
haticezehraferhatlar@gmail.com
05367387869

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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