ClinicalTrials.Veeva

Menu

Teletherapy for Upper Extremity Fracture Rehabilitation (TELE-REHAB Study)

University of Maryland Baltimore (UMB) logo

University of Maryland Baltimore (UMB)

Status

Withdrawn

Conditions

Upper Limb Surgery
Occupational Therapy

Treatments

Other: occupational therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT04691739
HP-00094373

Details and patient eligibility

About

Following upper limb surgeries, patients could receive occupational therapy either in-person or remotely (teletherapy). The investigators currently do not know which occupational therapy delivery is better in terms of clinical outcomes and patient recovery. The proposed study is a pilot randomized controlled trial (RCT) testing the feasibility of comparing in-person occupational therapy to teletherapy following operative fixation of upper extremity fracture. It is a single site, parallel-arm, randomized controlled trial to compare teletherapy versus in-person occupational therapy. Patients who are eligible will be randomized similar to a flip of a coin (1:1) to occupational therapy in-person or through a telemedicine platform. Patients would also complete surveys at each follow-up visit to measure clinical outcomes.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants must have had operative fixation of upper extremity fracture located between the humeral shaft and distal radius (inclusive) who are indicated for outpatient occupational therapy.
  • Participants at least 18 years (≥ 18 years of age).
  • English-speaking participants

Exclusion criteria

  • Participants unable to consent
  • Vulnerable populations including prisoners and marginally housed patients
  • Additional traumatic conditions that may affect the ultimate-use pattern of the injured limb including traumatic brain injury, spinal cord injury, peripheral nerve injury, or associated soft tissue injury requiring specific postoperative activity modifications.
  • Contralateral upper extremity injury that prevents participating in the standardized exercises.
  • Initiation of occupational therapy (OT) during an inpatient hospital stay
  • Pre-existing comorbidities that may interfere with communication or that may limit the use of standard telecommunications tools (sight/hearing impaired, speech impaired)
  • Patients without a smart-phone or internet access.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

In-person occupational therapy
Active Comparator group
Description:
occupational therapy delivered in-person
Treatment:
Other: occupational therapy
Teletherapy
Active Comparator group
Description:
Video-conferencing occupational therapy
Treatment:
Other: occupational therapy

Trial contacts and locations

1

Loading...

Central trial contact

Christopher Langhammer, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems