ClinicalTrials.gg
CompletedNCT07839533Updated Sep 28, 2026

Acupuncture as an Adjunct Treatment for Lateral Epicondylitis

An interventional study of Acupuncture and Kinesio Taping in Lateral Epicondylitis, sponsored by Enver Guven. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-09-28.

Sponsored by Enver Guven · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 5 months after the study started (first participant enrolled Apr 2025, registered Sep 2026).
Updated Sep 28, 2026Eligibility revisedInterventions changedGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Lateral epicondylitis, commonly known as tennis elbow, can cause pain and reduced hand and wrist function. This study evaluated whether adding acupuncture to a conservative rehabilitation program provides additional benefits for adults with lateral epicondylitis.

Participants were randomly assigned to one of two treatment groups. One group received acupuncture in addition to kinesio taping, a wrist orthosis, and a home exercise program. The other group received the same kinesio taping, wrist orthosis, and exercise program without acupuncture. Acupuncture was applied twice weekly for three weeks, for a total of six sessions.

Participants were assessed before treatment, at the end of the third week, and at three months. Outcomes included pain intensity, active wrist flexion and extension range of motion, pinch strength, and hand grip strength. The study aimed to determine whether acupuncture provides additional benefits when combined with standard conservative rehabilitation for lateral epicondylitis.

Read the detailed description

This was a prospective, single-center, two-arm randomized controlled clinical trial designed to evaluate the additional effects of acupuncture when combined with a standardized conservative rehabilitation program in adults with lateral epicondylitis.

Eligible adults aged 18 to 65 years with a clinical diagnosis of lateral epicondylitis and symptoms lasting at least six weeks were randomly allocated in a 1:1 ratio to two parallel treatment groups using a computer-generated randomization sequence. Allocation was concealed using sequentially numbered, opaque, sealed envelopes. Outcome assessments were performed by a blinded assessor.

The intervention group received acupuncture in addition to kinesio taping, a custom low-temperature thermoplastic volar wrist orthosis, and a home-based exercise program. Acupuncture was administered twice weekly for three weeks, for a total of six sessions. The acupuncture protocol included local, regional, and distal points and was performed by a physician trained in acupuncture.

Both groups received kinesio taping once weekly for three weeks, a custom volar wrist orthosis positioned at approximately 15-20 degrees of wrist extension for six weeks, and a home exercise program emphasizing eccentric wrist extensor strengthening and progressive grip exercises. Exercise performance and adherence were reviewed during follow-up visits.

Assessments were performed at baseline, at the end of week 3, and at month 3. The primary outcome was pain intensity measured using a 0-10 Visual Analog Scale. Secondary outcomes included active wrist flexion and extension range of motion measured with a goniometer, pinch strength measured with a pinch gauge, and hand grip strength measured with a Jamar hydraulic dynamometer. Adverse events related to acupuncture, kinesio taping, orthosis use, and exercise were also monitored throughout the study.

02

Conditions studied

  • Lateral Epicondylitis

Keywords

  • Tennis Elbow
  • Lateral Epicondylitis
  • Acupuncture
  • Kinesio Taping
  • Wrist Orthosis
  • Exercise Therapy
  • Rehabilitation
  • Pain
  • Grip Strength
  • Range of Motion
03

In context

Tennis Elbow

296 studies on the registry are indexed under Tennis Elbow; 64 are open to participants now.

This study's enrollment of 36 is below the median of 50 across 262 interventional studies indexed under Tennis Elbow.

Browse Tennis Elbow studies →

Lead sponsor

Enver Guven is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

The criteria were revised on the registry on Sep 28, 2026. See what changed

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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults aged 18 to 65 years
  • Clinical diagnosis of lateral epicondylitis
  • Symptoms of lateral epicondylitis lasting at least 6 weeks

Exclusion criteria

Exclusion Criteria:

  • injection to the affected elbow within the previous 6 months.
  • Previous elbow surgery.
  • Neurological disease affecting the tested upper limb.
  • Active cervical radiculopathy.
  • Systemic inflammatory disease.
  • Pregnancy.
  • Inability to comply with the study protocol or follow-up assessments.
Terms in these criteria, in plain language(1)

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.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
36 participants (actual)

Study arms

  • Experimental
    Adjunct Acupuncture + Multimodal Rehabilitation

    Participants received acupuncture in addition to kinesio taping, a custom volar wrist orthosis, and a home-based exercise program.

    Procedure: Acupuncture · Procedure: Kinesio Taping · Device: Volar Wrist Orthosis · Behavioral: Home-Based Exercise Program

  • Active comparator
    Multimodal Rehabilitation Without Acupuncture

    Participants received kinesio taping, a custom volar wrist orthosis, and a home-based exercise program without acupuncture.

    Procedure: Kinesio Taping · Device: Volar Wrist Orthosis · Behavioral: Home-Based Exercise Program

Interventions

  • ProcedureAcupuncture

    Acupuncture was administered twice weekly for 3 weeks, for a total of 6 sessions. Local and regional points included Ah-shi, Large Intestine 10 (LI10), Large Intestine 11 (LI11), and Lung 5 (LU5); distal and segmental points included Large Intestine 4 (LI4), San Jiao 5 (SJ5), Small Intestine 3 (SI3), Gallbladder 34 (GB34), and Liver 3 (LIV3). Sterile filiform needles were retained for 20-25 minutes and manually stimulated at approximately 5-minute intervals to elicit or maintain deqi.

  • ProcedureKinesio Taping

    Kinesio taping was applied once weekly for 3 weeks. A 5-cm elastic therapeutic tape was applied with no stretch on the anchors and approximately 15-25% stretch over the therapeutic segments. An X/donut strip was centered over the lateral epicondyle and a Y-strip was applied along the wrist extensor muscle group.

  • DeviceVolar Wrist Orthosis

    A custom low-temperature thermoplastic volar wrist cock-up orthosis was fabricated with the wrist positioned at approximately 15-20 degrees of extension. Participants were instructed to wear the orthosis during daytime activities for 6 weeks, removing it for hygiene and skin checks.

  • BehavioralHome-Based Exercise Program

    The home-based exercise program focused on eccentric wrist extensor strengthening and progressive grip exercises. Eccentric wrist extension was initiated with 0.5 kg and progressed in repetitions and load. Grip exercises using therapeutic putty were progressively performed with the elbow flexed and then extended, in supination, neutral, and pronation positions.

06

What researchers measure

Primary outcomes

  1. Change in Pain Intensity From Baseline to Month 3

    Pain intensity was assessed using a 0-10 Visual Analog Scale (VAS), where 0 represents no pain and 10 represents the worst imaginable pain. The primary endpoint was the between-group difference in change in VAS pain from baseline to Month 3.

    Time frame: Baseline and Month 3

Secondary outcomes

  1. Change in Active Wrist Flexion Range of Motion

    Active wrist flexion range of motion was measured in degrees using a standard goniometer. Three measurements were obtained at each assessment and the mean value was analyzed.

    Time frame: Baseline, Week 3, and Month 3

  2. Change in Active Wrist Extension Range of Motion

    Active wrist extension range of motion was measured in degrees using a standard goniometer. Three measurements were obtained at each assessment and the mean value was analyzed.

    Time frame: Baseline, Week 3, and Month 3

  3. Change in Pinch Strength

    Pinch strength was measured in kilograms using a Baseline® pinch gauge in a standardized position. Three measurements were obtained at each assessment and the mean value was analyzed.

    Time frame: Baseline, Week 3, and Month 3

  4. Change in Hand Grip Strength

    Hand grip strength was measured in kilograms using a Jamar hydraulic dynamometer in a standardized position. Three measurements were obtained at each assessment and the mean value was analyzed.

    Time frame: Baseline, Week 3, and Month 3

07

Study locations

1 site
  • Traditional and Complementary Medicine Clinic
    Ankara, Ankara, Turkey (Türkiye)
08

References and documents

Publications

  • MacPherson H, Altman DG, Hammerschlag R, Li Y, Wu T, White A, Moher D; STRICTA Revision Group. Revised STandards for Reporting Interventions in Clinical Trials of Acupuncture (STRICTA): extending the CONSORT statement. Acupunct Med. 2010 Jun;28(2):83-93. doi: 10.1136/aim.2009.001370. Epub 2010 Jun 8. PubMed 20615861 ↗
  • McQueen KS, Powell RK, Keener T, Whalley R, Calfee RP. Role of strengthening during nonoperative treatment of lateral epicondyle tendinopathy. J Hand Ther. 2021 Oct-Dec;34(4):619-626. doi: 10.1016/j.jht.2020.10.009. Epub 2020 Oct 16. PubMed 33250396 ↗
  • Fink M, Wolkenstein E, Karst M, Gehrke A. Acupuncture in chronic epicondylitis: a randomized controlled trial. Rheumatology (Oxford). 2002 Feb;41(2):205-9. doi: 10.1093/rheumatology/41.2.205. PubMed 11886971 ↗
  • Shin KM, Kim JH, Lee S, Shin MS, Kim TH, Park HJ, Lee MH, Hong KE, Lee S, Choi SM. Acupuncture for lateral epicondylitis (tennis elbow): study protocol for a randomized, practitioner-assessor blinded, controlled pilot clinical trial. Trials. 2013 Jun 14;14:174. doi: 10.1186/1745-6215-14-174. PubMed 23768129 ↗

Individual participant data

Plan to share: Yes — De-identified individual participant data underlying the results reported in this study may be made available upon reasonable request to the corresponding author. Data will be shared only in a form that protects participant confidentiality.

Time frame: Data will be available beginning after publication of the study results and for 5 years following publication.

Access criteria: De-identified data will be available to qualified researchers who submit a reasonable written request to the corresponding author describing the purpose of the proposed analysis. Requests will be reviewed by the study investigators. Data will be shared only for scientifically appropriate purposes and in accordance with participant confidentiality and applicable ethical requirements.

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

Ran from Apr 2025 to primary completion in Sep 2025, 5 months.

Of 152 non-industry interventional studies with no phase under Tennis Elbow, half reached primary completion within 8 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 24. This study's 5 months is below that.

Counting every sponsor, half of 154 studies reached it within 8 months; a quarter within 5 and three quarters within 22.

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

Registered
Sep 19, 2026
First posted
Sep 24, 2026
StartActual
Apr 5, 2025
Primary completionActual
Sep 12, 2025
CompletionActual
Sep 12, 2025
Last update
Sep 28, 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.
Eligibility
1 inclusion criterion edited, 2 added; 2 exclusion criteria edited, 5 added
What changed in the criteria
Inclusion criteria
  • AddedAdults aged 18 to 65 years
  • AddedClinical diagnosis of lateral epicondylitis
  • EditedInclusion Criteria: Adults aged 18 to 65 years. Clinical diagnosis of lateral epicondylitis. Symptoms of lateral epicondylitis lasting at least 6 weeks.
Exclusion criteria
  • EditedExclusion Criteria: Steroid injection to the affected elbow within the previous 6 months.
  • AddedPrevious elbow surgery.
  • AddedNeurological disease affecting the tested upper limb.
  • AddedActive cervical radiculopathy.
  • AddedSystemic inflammatory disease.
  • AddedPregnancy.
  • EditedPrevious elbow surgery. Neurological disease affecting the tested upper limb. Active cervical radiculopathy. Systemic inflammatory disease. Pregnancy. Inability to comply with the study protocol or follow-up assessments.
Sep 28, 2026
Interventions
Arm changed Arm 1→Adjunct Acupuncture + Multimodal Rehabilitation; Arm 2→Multimodal Rehabilitation Without Acupuncture
Sep 28, 2026
Show all 1 update
  1. Sep 28, 2026
    Eligibility 1 inclusion criterion edited, 2 added; 2 exclusion criteria edited, 5 added
    What changed in the criteria
    Inclusion criteria
    • AddedAdults aged 18 to 65 years
    • AddedClinical diagnosis of lateral epicondylitis
    • EditedInclusion Criteria: Adults aged 18 to 65 years. Clinical diagnosis of lateral epicondylitis. Symptoms of lateral epicondylitis lasting at least 6 weeks.
    Exclusion criteria
    • EditedExclusion Criteria: Steroid injection to the affected elbow within the previous 6 months.
    • AddedPrevious elbow surgery.
    • AddedNeurological disease affecting the tested upper limb.
    • AddedActive cervical radiculopathy.
    • AddedSystemic inflammatory disease.
    • AddedPregnancy.
    • EditedPrevious elbow surgery. Neurological disease affecting the tested upper limb. Active cervical radiculopathy. Systemic inflammatory disease. Pregnancy. Inability to comply with the study protocol or follow-up assessments.
    Interventions Arm changed Arm 1→Adjunct Acupuncture + Multimodal Rehabilitation; Arm 2→Multimodal Rehabilitation Without Acupuncture

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
NCT07839533
Lead sponsor
Enver Guven
Responsible party
Enver Guven (Assistant Professor, Ankara University) — Sponsor-investigator
First posted
Sep 24, 2026
Start date
Apr 5, 2025
Primary completion
Sep 12, 2025
Completion
Sep 12, 2025
Last update
Sep 28, 2026

Study contacts

Enver Guven, PhD
principal investigator · Ankara University

Oversight

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

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