Feasibility and Acceptability of Integrative Therapy for Managementof Symptomsin Persons With Pulmonary Hypertension

2.50
Hdl Handle:
http://hdl.handle.net/10755/620221
Category:
Full-text
Type:
Poster
Title:
Feasibility and Acceptability of Integrative Therapy for Managementof Symptomsin Persons With Pulmonary Hypertension
Author(s):
Von Visger, Tania; Thrane, Susan; Klatt, Maryanna; Dabbs, Annette; Chlan, Linda; Happ, Mary Beth
Lead Author STTI Affiliation:
Epsilon
Author Details:
Tania Von Visger, APRN, CNS, CCNS, PCCN, von-visger@osu.edu; Susan Thrane, RN; Maryanna Klatt; Annette Dabbs, RN; Linda Chlan, RN; Mary Beth Happ, RN, FAAN, FGSA
Abstract:
Session presented on Sunday, September 18, 2016: Background: Persons with the life-limiting cardiopulmonary disease face many symptom management challenges. Pulmonary Hypertension (PH) is one such progressive and debilitating chronic condition and serves as an excellent model for symptom management intervention development and testing. High mean pulmonary pressure characteristic of PH and the medications used to treat the disease lead to distressing symptoms such as chest pain, anxiety, nausea, insomnia, dyspnea, dizziness, and fatigue. Increased symptom burden can impair patients? ability to manage and adhere to medical treatments leading to reduced quality of life. Integrative approaches to symptom management are urgently needed. Many integrative health approaches have shown benefit in symptom alleviation in chronic conditions such as cancer and heart disease and may have therapeutic benefits in severe cardiopulmonary conditions such as PH. A patient-centered, pragmatic integrative approach to symptom treatment can provide holistic management without added side effects. The purpose of this mixed-methods pilot study is to determine the feasibility, acceptability, and preliminary efficacy of a 6-week integrative therapy program, Urban Zen Integrative Therapy (UZIT) among community-dwelling adults with PH. Methods: The presentation will describe methods of determining the feasibility of a 6-week UZIT intervention in community-dwelling adults with PH. Feasibility will be determined by 1) Recruitment rate (>40% recruited from those approached), 2) Enrollment rate (>two /month), 3) Home practice (> 1/week), and 4) retention rate (>70% of participants remaining at study completion). The presentation will describe methods of determining the acceptability of UZIT among community-dwelling adults with PH for symptom management. Acceptability will be determined by 1) Participants? evaluation of the UZIT program (composite mean System Usability Scale score > 5, scale 1-7), 2) Session completion rate (at least 5 of 6 sessions [83% attendance] by the participants retained at the study end), and 3) An exploratory sub-aim (Aim 2-A) is to determine what components of the UZIT program are preferred by adults with PH. The presentation will describe strategies in maximizing intervention fidelity of a UZIT intervention that will include: consistency of intervention delivery and intervention dose. To strengthen the study design, we will address: 1) research intervention protocol, 2) interventionists? competency training, 3) quality audit, and 4) research process evaluation. The study will enroll a single cohort of 20 patients with PH at The Ohio State University Wexner Medical Center PH outpatient clinics who are willing to participate in 6 weekly-60-minutes sessions of UZIT. The UZIT intervention will include four integrative modalities: essential oil, gentle body movement/restorative pose, body-awareness meditation, and Reiki. A trained UZIT therapist will provide treatments tailored to patients? symptoms and physical capability, within the bounds of the research protocol. Qualitative and quantitative data will be used to assess the feasibility and acceptability of the UZIT intervention. Field notes, semi-structured interviews, and daily symptom diaries will provide a qualitative description of symptoms and UZIT acceptability and constant comparison. Intervention sessions will be remotely video recorded and examined for fidelity. Discussion: Implementation of behavioral intervention is challenged by many threats to study?s internal validity. Furthermore, mind-body integrative therapy with multi-modal components (UZIT) adds complexity to the scientific testing standards. Measuring ways to assure that the intervention is feasible and acceptable to participants and that the intervention delivery dose is consistent will optimize scientific rigor. In preparation for future efficacy testing of this intervention, these basic requirements proposed in this preliminary testing detailing the design and implementation of UZIT research for symptom management in cardiopulmonary illness is necessary. If feasible and acceptable to cardiopulmonary patients, this intervention has the potential to mitigate the bothersome symptoms inherent in life-limiting, cardiopulmonary diseases and improve patients? quality of life. This presentation will use the exemplar of UZIT integrative therapy for symptom management in patients with pulmonary hypertension.
Keywords:
Symptom Mangement; Integrative Therapy; Acceptability
Repository Posting Date:
16-Sep-2016
Date of Publication:
16-Sep-2016
Other Identifiers:
LEAD16PST77
Conference Date:
2016
Conference Name:
Leadership Connection 2016
Conference Host:
Sigma Theta Tau International
Conference Location:
Indianapolis, Indiana, USA
Description:
Leadership Connection 2016 Theme: Personal. Professional. Global. Held at the Marriott Downtown, Indianapolis.

Full metadata record

DC FieldValue Language
dc.language.isoen_USen
dc.type.categoryFull-texten
dc.typePosteren
dc.titleFeasibility and Acceptability of Integrative Therapy for Managementof Symptomsin Persons With Pulmonary Hypertensionen
dc.contributor.authorVon Visger, Taniaen
dc.contributor.authorThrane, Susanen
dc.contributor.authorKlatt, Maryannaen
dc.contributor.authorDabbs, Annetteen
dc.contributor.authorChlan, Lindaen
dc.contributor.authorHapp, Mary Bethen
dc.contributor.departmentEpsilonen
dc.author.detailsTania Von Visger, APRN, CNS, CCNS, PCCN, von-visger@osu.edu; Susan Thrane, RN; Maryanna Klatt; Annette Dabbs, RN; Linda Chlan, RN; Mary Beth Happ, RN, FAAN, FGSAen
dc.identifier.urihttp://hdl.handle.net/10755/620221-
dc.description.abstractSession presented on Sunday, September 18, 2016: Background: Persons with the life-limiting cardiopulmonary disease face many symptom management challenges. Pulmonary Hypertension (PH) is one such progressive and debilitating chronic condition and serves as an excellent model for symptom management intervention development and testing. High mean pulmonary pressure characteristic of PH and the medications used to treat the disease lead to distressing symptoms such as chest pain, anxiety, nausea, insomnia, dyspnea, dizziness, and fatigue. Increased symptom burden can impair patients? ability to manage and adhere to medical treatments leading to reduced quality of life. Integrative approaches to symptom management are urgently needed. Many integrative health approaches have shown benefit in symptom alleviation in chronic conditions such as cancer and heart disease and may have therapeutic benefits in severe cardiopulmonary conditions such as PH. A patient-centered, pragmatic integrative approach to symptom treatment can provide holistic management without added side effects. The purpose of this mixed-methods pilot study is to determine the feasibility, acceptability, and preliminary efficacy of a 6-week integrative therapy program, Urban Zen Integrative Therapy (UZIT) among community-dwelling adults with PH. Methods: The presentation will describe methods of determining the feasibility of a 6-week UZIT intervention in community-dwelling adults with PH. Feasibility will be determined by 1) Recruitment rate (>40% recruited from those approached), 2) Enrollment rate (>two /month), 3) Home practice (> 1/week), and 4) retention rate (>70% of participants remaining at study completion). The presentation will describe methods of determining the acceptability of UZIT among community-dwelling adults with PH for symptom management. Acceptability will be determined by 1) Participants? evaluation of the UZIT program (composite mean System Usability Scale score > 5, scale 1-7), 2) Session completion rate (at least 5 of 6 sessions [83% attendance] by the participants retained at the study end), and 3) An exploratory sub-aim (Aim 2-A) is to determine what components of the UZIT program are preferred by adults with PH. The presentation will describe strategies in maximizing intervention fidelity of a UZIT intervention that will include: consistency of intervention delivery and intervention dose. To strengthen the study design, we will address: 1) research intervention protocol, 2) interventionists? competency training, 3) quality audit, and 4) research process evaluation. The study will enroll a single cohort of 20 patients with PH at The Ohio State University Wexner Medical Center PH outpatient clinics who are willing to participate in 6 weekly-60-minutes sessions of UZIT. The UZIT intervention will include four integrative modalities: essential oil, gentle body movement/restorative pose, body-awareness meditation, and Reiki. A trained UZIT therapist will provide treatments tailored to patients? symptoms and physical capability, within the bounds of the research protocol. Qualitative and quantitative data will be used to assess the feasibility and acceptability of the UZIT intervention. Field notes, semi-structured interviews, and daily symptom diaries will provide a qualitative description of symptoms and UZIT acceptability and constant comparison. Intervention sessions will be remotely video recorded and examined for fidelity. Discussion: Implementation of behavioral intervention is challenged by many threats to study?s internal validity. Furthermore, mind-body integrative therapy with multi-modal components (UZIT) adds complexity to the scientific testing standards. Measuring ways to assure that the intervention is feasible and acceptable to participants and that the intervention delivery dose is consistent will optimize scientific rigor. In preparation for future efficacy testing of this intervention, these basic requirements proposed in this preliminary testing detailing the design and implementation of UZIT research for symptom management in cardiopulmonary illness is necessary. If feasible and acceptable to cardiopulmonary patients, this intervention has the potential to mitigate the bothersome symptoms inherent in life-limiting, cardiopulmonary diseases and improve patients? quality of life. This presentation will use the exemplar of UZIT integrative therapy for symptom management in patients with pulmonary hypertension.en
dc.subjectSymptom Mangementen
dc.subjectIntegrative Therapyen
dc.subjectAcceptabilityen
dc.date.available2016-09-16T14:22:36Z-
dc.date.issued2016-09-16-
dc.date.accessioned2016-09-16T14:22:36Z-
dc.conference.date2016en
dc.conference.nameLeadership Connection 2016en
dc.conference.hostSigma Theta Tau Internationalen
dc.conference.locationIndianapolis, Indiana, USAen
dc.descriptionLeadership Connection 2016 Theme: Personal. Professional. Global. Held at the Marriott Downtown, Indianapolis.en
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