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NCT04401943Completed

Online Fatigue Intervention Program for People With Scleroderma

Pilot Study of an Online Fatigue Intervention Program for People With Scleroderma

Source: ClinicalTrials.gov · Last updated 26 Jun 2024

Brief summary (registry, in English)

This research is being done to evaluate if an online fatigue intervention program will decrease fatigue, pain and increase confidence managing fatigue and being able to do daily tasks. This study involves competing a series of questionnaires before and after the intervention , and attending and participating in the online videoconference fatigue program for 1 1/2 hour meetings each week over a 6-week period of time.

Status (registry)
Completed
Study type
Interventional
Enrollment
12 (actual)
First submitted
13 May 2020
Start date
13 May 2020
Primary completion date
31 Mar 2024
Lead sponsor
University of New Mexico
NCT number
NCT04401943

What you commit to

  • Study type: Interventional
  • Participants enrolled: 12
  • From 13 May 2020 to the primary completion date, 31 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Pregnancy
  • Not having use of a device with internet, email access, and video conferencing capabilities (both audio and visual)
  • Not able to communicate in English
  • Score \< 12 on the fatigue screening questions
  • Not willing or not able to complete the study protocol or participate in the program at the designated times and days.

Who the study is looking for

  • Resident of the United States
  • Diagnosis of systemic scleroderma
  • 18 years of age or older
  • Have use of a device with internet and email access, and video conferencing capabilities (both audio and visual)
  • Communicate in English
  • Have fatigue (combined score of \>12 on 3 questions that rate degree of fatigue, severity of fatigue, and level of stress caused by fatigue on a scale from 1 - 10)
  • Be willing and available to complete the study protocol which consists of attending a 1.5 hour virtual meeting once a week for 6 weeks.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of New Mexico
Coordinator of this site? Confirm its status
AlbuquerqueUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.