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Therapeutic effects of manual therapy, transcutaneous electric nerval stimulation und forearm (extensor) brace on lateral epicondylopathia - a randomized controlled trial

Therapeutic effects of manual therapy, transcutaneous electric nerval stimulation und forearm (extensor) brace on lateral epicondylopathia - a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00021137
Enrollment
52
Registered
2020-03-24
Start date
2013-01-10
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

M77.1

Interventions

Group 1: manual therapy Group 2: TENS, forearm brace Group 3: manual therapy, TENS, forearm brace

Sponsors

Praxis für Allgemeinmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients were included in the order they appeared at the practice with no pre-selection if they met the following criteria: (1) age between 18 and 65 years, (2) criteria for the diagnosis of a lateral epicondylitis needed to be fulfilled, (3) informed consent was given. Lateral epicondylopathia was diagnosed if (1) pain was reported for the lateral region of the elbow, (2) an extension of the hand joint provoked significant pain (provocation test), and (3) other diseases or injuries were excluded.

Exclusion criteria

Exclusion criteria: Patients were excluded from the study if they met at least one of the following criteria: injuries reported for the arm or cervical spine during the last 6 months, acute or chronic infections, rheumatic diseases, osteochondrosis dissecans, advanced osteoarthritis in the elbow, pregnancy, diabetes, malignoms, medication with beta blockers, medication with statins, malformation in upper extremities, circulatory disorder in upper extremities, radicular syndrome (C 6), chronic pain syndrome, manifest psychiatric disorder, neuropathy, myopathy.

Design outcomes

Primary

MeasureTime frame
Primary Outcomes were measured: Pain with VAS (visual analogous scale) and Range of Motion (ROM) of of the elbow joint in degrees before treatment (0) and in three follow ups 4, 8 weeks and 1 year later

Secondary

MeasureTime frame
Secondary Outcomes were measured: Pain and Range of Motion with PRTEE (Patient Rated Tennis Elbow Evaluation Questionnaire) and psychosocial well-being with the Sf 36 (Short form 36 Questionnaire) before treatment (0) and in three follow ups 4, 8 weeks and 1 year later

Countries

Germany

Contacts

Public ContactWolfgang Rachold

Praxis für Allgemeinmedizin

wrachold@me.com00491779773380

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026