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临床试验/NCT04691739
NCT04691739撤回不适用

Teletherapy for Upper Extremity Fracture Rehabilitation, A Pilot Randomized Controlled Trial (TELE-REHAB Study)

University of Maryland, Baltimore1 个研究点 分布在 1 个国家开始时间: 2022年1月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Feasibility outcome 2b: Completion rate

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •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.

研究组 & 干预措施

In-person occupational therapy

Active Comparator

occupational therapy delivered in-person

干预措施: occupational therapy (Other)

Teletherapy

Active Comparator

Video-conferencing occupational therapy

干预措施: occupational therapy (Other)

结局指标

主要结局

Feasibility outcome 2b: Completion rate

时间窗: at 3 months

A success threshold of 90% patient follow-up and case report forms

Feasibility outcome 2c: Completion rate

时间窗: at 6 months

A success threshold of 90% patient follow-up and case report forms

Feasibility outcome 1: Enrollment rate

时间窗: At 12 months

A success threshold of 40% enrollment of eligible patients

Feasibility outcome 2a: Completion rate

时间窗: at 6 weeks

A success threshold of 90% patient follow-up and case report forms completion rates

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Christopher Langhammer

Assistant Professor

University of Maryland, Baltimore

研究点 (1)

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