A Comparison of Accelerometers for Measuring Daily Activity in Sarcoid

NCT ID: NCT02626897

Last Updated: 2015-12-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-01-31

Study Completion Date

2016-05-31

Brief Summary

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This cross-over study of 12 patients with sarcoidosis will look at two different widely-used accelerometer devices. These devices are wrist worn and similar in size to a wrist-watch. They measure daily activity levels. The investigators hope to use one of these devices in the future within a randomised-controlled trial looking at using methylphenidate for the treatment of sarcoidosis-associated fatigue. In order to ensure that the investigators choose the ideal device the investigators wish to compare the GENEActiv and ActiGraph GT3X devices. Participants will be required to wear the devices for 7 days each, with 6 patients beginning with the GENEActiv device and changing to the ActiGraph device after 7 days, the remaining 6 participants starting with the Actigraph before changing to the GENEActiv. Patients will complete a short exit questionnaire about their experience with the devices and their preference. The best device will be determined by both patient preference and reliability of collecting data.

Detailed Description

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This will be a small comparator study comparing two devices (GENEActiv original and ActiGraph GT3X) in 12 patients with sarcoidosis. Participants wear one device for 7 days before returning the device, and wear the second device to wear for a further 7 day period. Each participant will wear the devices for 24 hours throughout the measurement period. The devices will be worn in a random order, randomised using sealed envelopes. They will be advised not to remove the devices during the 7 day monitoring period, with the exception of the GT3X which should be removed if the participant is bathing or swimming (they are able to shower). When each device is returned the participants will be asked to complete an exit questionnaire on their experience with the device. Before the participants wear the devices they will be asked to complete a short question regarding how tired/fatigued they feel.

The devices will be worn on the participant's non-dominant wrist. They will wear both devices in a random order (determined by randomisation at the start of the trial with regards to which device will be worn first). Six participants will start with the GENEActiv device and six will begin with the Actigraph GT3X device. The device order will be chosen randomly based upon a random number sequence generated in Microsoft Excel and placed in envelopes numbered 1 to 12.

Conditions

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Sarcoidosis

Keywords

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Sarcoidosis Daily activity Exercise Accelerometer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Blinding Strategy

NONE

Study Groups

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Sarcoidosis - GENEActiv device first

Six patients start with the GENEActiv wrist-worn accelerometer which is needed to be worn for a 7 day period. Participants then switch to the ActiGraph GT3X device for a 7 day period. At the end of this second period they complete a short exit questionnaire detailing their experience and their device preference.

Group Type OTHER

GENEActiv Original Accelerometer

Intervention Type DEVICE

Wrist-worn device measuring accelerations as a measure of daily activity.

ActiGraph GT3X Accelerometer

Intervention Type DEVICE

Wrist-worn device measuring accelerations as a measure of daily activity.

Sarcoidosis - ActiGraph device first

Six patients start with the ActiGraph GT3X wrist-worn accelerometer which is needed to be worn for a 7 day period. Participants then switch to the GENEActiv device for a 7 day period. At the end of this second period they complete a short exit questionnaire detailing their experience and their device preference.

Group Type OTHER

GENEActiv Original Accelerometer

Intervention Type DEVICE

Wrist-worn device measuring accelerations as a measure of daily activity.

ActiGraph GT3X Accelerometer

Intervention Type DEVICE

Wrist-worn device measuring accelerations as a measure of daily activity.

Interventions

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GENEActiv Original Accelerometer

Wrist-worn device measuring accelerations as a measure of daily activity.

Intervention Type DEVICE

ActiGraph GT3X Accelerometer

Wrist-worn device measuring accelerations as a measure of daily activity.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Male or Female aged over 18
2. Diagnosed with sarcoidosis by either; biopsy confirming non-caseating granulomas consistent with sarcoidosis, or multi-disciplinary interstitial lung disease meeting diagnosis of sarcoidosis.
3. Ambulatory patient (not wheelchair or bed-bound)
4. Able to provide written informed consent

Exclusion Criteria

1\. Unable to provide informed consent.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of East Anglia

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chris Atkins, MB/BS

Role: PRINCIPAL_INVESTIGATOR

University of East Anglia

Andrew M Wilson, MD

Role: STUDY_DIRECTOR

University of East Anglia

Locations

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Norfolk and Norwich Univeristy Hospital NHS foundation Trust

Norwich, Norfolk, United Kingdom

Site Status

Countries

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United Kingdom

Central Contacts

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Chris Atkins, MB/BS

Role: CONTACT

Phone: 01603591594

Email: [email protected]

Other Identifiers

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1.3-27.11.2015

Identifier Type: -

Identifier Source: org_study_id