The Feasibility of the PAINReportIt Guided Relaxation Intervention-Outpatient

NCT ID: NCT02729363

Last Updated: 2020-01-22

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

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-04-30

Study Completion Date

2017-03-01

Brief Summary

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Our goal is to improve the self-management of pain and stress in adult outpatients with sickle cell disease (SCD) by determining the feasibility of a self-managed guided relaxation (GR) stress reduction intervention using a tablet-based mobile device. Currently, opioid analgesics are primarily used to treat SCD pain while self-managed behavioral modalities such as GR, are rarely used. Little is known about the effects or mechanisms of GR on pain and stress, in adults with SCD. Emerging evidence from the hypothalamic pituitary adrenal (HPA) axis theory offer insights for understanding the mechanisms. Adding GR as a supplement to analgesic therapies will address the paucity of self-management strategies for controlling pain in SCD. GR is a simple and cost-effective non-drug intervention that could reduce pain and stress in outpatients with SCD. GR is an intervention where outpatients with SCD are directed to listen to and view audio-visual recordings while they visualize themselves being immersed in that scene.

Detailed Description

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The investigator will recruit adult outpatients with sickle cell disease (SCD) from the University of Florida Health Hematology Clinics and conduct study visits in a research room located at the College of nursing.

The investigator will stratify participants on worst pain intensity (\<=5 and \>5) and randomly assign 15 adults to attention control (stress/pain tracking; 12-min SCD experience discussion) and 15 adults to experimental (stress/pain tracking; 12-min GR video clip) groups.

The immediate intervention effects will be examined for pain (primary) and stress (secondary) outcomes. Vital signs for determining relaxation responses (mediators) will be collected immediately before and after the 12-min interventions.

Conditions

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Sickle Cell Disease Stress Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Guided Relaxation video clip

This intervention is a 12-minute guided audio-visual relaxation intervention delivered at the baseline visit to determine the immediate effects of guided relaxation intervention on stress and pain in outpatients with sickle cell disease.

Group Type EXPERIMENTAL

Guided Relaxation video clip

Intervention Type BEHAVIORAL

This intervention is a 12-minute guided audio-visual relaxation intervention.

Sickle cell experience discussion

Attention Control Group: This intervention is a 12-minute sickle cell disease experience discussion. In this computer-based discussion, patients talk about their sickle cell disease experience. The audio-taped questions and onscreen directions were programmed for self-administration. Subjects' responses will be captured via the microphone so that Data Collectors are not involved in this discussion process, and it is equivalent to the guided relaxation activity.

Group Type OTHER

Sickle Cell Disease Experience Discussion

Intervention Type BEHAVIORAL

This intervention is a 12-minute computer-administered sickle cell disease experience discussion.

Interventions

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Guided Relaxation video clip

This intervention is a 12-minute guided audio-visual relaxation intervention.

Intervention Type BEHAVIORAL

Sickle Cell Disease Experience Discussion

This intervention is a 12-minute computer-administered sickle cell disease experience discussion.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Has SCD diagnosis;
* Reports pain 3 or greater in the previous 24 hours (0-10 scale)
* Receives care at the University of Florida (UF) Health/Shands
* Speaks and reads English
* 18 years of age or older
* Self-identifies as being of African or Hispanic descent

Exclusion Criteria

* Legally blind
* Physically or cognitively unable to complete study measures
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Florida

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Miriam O Ezenwa, PhD, RN

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Locations

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University of Florida Hematology Clinic-Medical Plaza

Gainesville, Florida, United States

Site Status

Countries

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United States

References

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Ezenwa MO, Yao Y, Nguyen MT, Mandernach MW, Hunter CT, Yoon SL, Fedele D, Lucero RJ, Lyon D, Wilkie DJ. Randomized Pilot Study: A Mobile Technology-based Self-management Intervention for Sickle Cell Pain. West J Nurs Res. 2020 Aug;42(8):629-639. doi: 10.1177/0193945919878821. Epub 2019 Oct 4.

Reference Type DERIVED
PMID: 31583977 (View on PubMed)

Other Identifiers

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IRB201600042

Identifier Type: -

Identifier Source: org_study_id

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