/
The Implications of CAPS Biofeedback Research on Treatment Strategies: The Implications of CAPS Biofeedback Research on Treatment Strategies:

The Implications of CAPS Biofeedback Research on Treatment Strategies: - PowerPoint Presentation

reportperfect
reportperfect . @reportperfect
Follow
343 views
Uploaded On 2020-06-16

The Implications of CAPS Biofeedback Research on Treatment Strategies: - PPT Presentation

Cutting Edge HRV Training Stress Management and Biofeedback Services Counseling and Psychological Services CAPS Brigham Young University Faculty Training Maureen Rice Barbara Morrell Yoko Caldwell Meredith Pescatello Tristin Roney Louise Wheeler Lisa Leavitt ID: 779345

amp biofeedback stress heart biofeedback amp heart stress acc rate follow time hrv amyg hipp depression baseline groups significant

Share:

Link:

Embed:

Download Presentation from below link

Download The PPT/PDF document "The Implications of CAPS Biofeedback Res..." is the property of its rightful owner. Permission is granted to download and print the materials on this web site for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.


Presentation Transcript

Slide1

The Implications of CAPS Biofeedback Research on Treatment Strategies: Cutting Edge HRV Training

Stress Management and Biofeedback Services

Counseling and Psychological Services (CAPS)

Brigham Young University

Faculty Training

Maureen Rice, Barbara Morrell, Yoko Caldwell, Meredith Pescatello, Tristin Roney, Louise Wheeler, Lisa Leavitt,

Dianne Nielsen

Slide2

www.themegallery.com

STUDY #1 – AAPBThe Efficacy of Stress Management and Biofeedback Training as an Adjunct to Psychotherapy for University StudentsMorrell, B., Nielsen, D., Rice, M., Erekson, D., Marvin, L., Brown, L.

Slide3

OQ-45 Administered before every counseling sessionItems heavily loaded on stress and anxietyI tire quicklyI feel stressed at work/school.I feel fearfulI have difficulty concentrating.My heart pounds too much

I feel nervousI have trouble falling asleep or staying asleepI have headachesI have sore muscles

Slide4

Therapy Outcome for CAPS Clients Receiving No Biofeedback, One session, and Multiple Sessions Significant differences were found between groups on total OQ-45 change from 2008 to 2012 (p = .018)

1 or less biofeedback sessions averaged 8 points of change2+ biofeedback sessions averaged 11 points of change

Slide5

Additionally, a multilevel analysis of biofeedback and outcome on the OQ-45 from 1996 to 2012 found that the

total number of biofeedback sessions in a course of therapy predicted a faster decrease in OQ-45 scores (p = .005), controlling for initial severity on the OQ

Slide6

www.themegallery.com

Study #2 – AAPBImpact of Resonant Frequency HRV Training in the Treatment of Depression and Resting-state fMRIYoko H. W. Caldwell

Brigham Young University

Dissertation

Slide7

Depression & Brain Functioning

Structural & Functional dysfunctioning

Volume reduction – hippocampus & amygdala

(Drevets, 2001; Mervaala et al., 2000)

Decreased connectivity

Functional – prefrontal cortex & ACC

(Aizenstein et al., 2009)

Resting-state – ACC, hippocampus, amygdala, orbitofrontal & prefrontal cortex

(Anand et al., 2005; Lui et al., 2011)

Slide8

MDD TxMeds

(Rush et al., 2006)Therapy(Butler, Chapman, Forman, & Beckm, 2006)

Adjunct Therapy

(Amr, El-Mogy, Shams, Vieira, & Lakhan, 2013; Tonhajzerova et al., 2009)

Slide9

Heart-Rate Variability (HRV)

HRV & Health OutcomeSympathetic Parasympathetic activity (Beevers, Ellis, & Reid, 2011)Associated with positive health outcome

Cardiac morbidity

(Del Pozo et al., 2004)

Pulmonary function

(Lehrer et al., 2003)

Chronic pain

(Hallman, Olsson, Scheele, Melin, & Lyskov, 2011)

Depressive disorders

(Karavidas et al., 2007)

Slide10

The Current StudyPurposeExamine impact of HRV training on depressive symptoms and resting-state connectivity

ROIs: ACC, hippocampus & amygdala

Slide11

MethodParticipantsExclusion: age <18 or > 25 yrs, Hx of major illness, cardiovascular dx, substance abuse

Females (N = 32) MDD participants: BYU Counseling CenterHealthy participants: BYU campus

Excluded 2 participants

Final sample size: n = 30

$20 – each MRI visit; $10 – each HRV visit

Slide12

Participants (cont’)

Age M = 20.09 M = 20.20 M = 20.64 SD = 1.81 SD = 1.47 SD = 1.29

Both Tx & HRV

Tx only

Active control

Slide13

MeasuresPsychologicalM.I.N.I International Neuropsychiatric Interview

(Sheehan et al., 1998)Beck Depression Inventory-II (BDI-II) (Beck, Steer, & Brown, 1996)Outcome Questionnaire-45 (OQ45) (Lambert, 1994)

Physiological for HRV

Biofeedback system (J&J)

Standard deviation of normal-to-normal intervals (SDNN)

High frequency (HF)

Low frequency (LF)

LF/HF ratio

Slide14

Physiological variablesSDNN Amount of variability in heartbeat interval across timeHF and LF

LF/HF ratio

0.15

0.4

0.05

Slide15

MRI ScannerBYU MRI RFSiemens 3T Tim Trio MR scannerFunctional imagesStructural images

Slide16

ProcedureRecruitment phaseM.I.N.IExperimental phase

Slide17

Capture the Moments

Slide18

Analytic StrategyRepeated measure ANOVA3 (Exp, TAU, Ch) x 2 (Baseline, follow-up)BDI-IIOQ-45All HRV variables (SDNN, LF, HF, LF/HF)LF, HF, LF/HF

 Log10 transformationResting-state connectivity between each ROIs

Slide19

Results- Baseline

Group differenceF(2, 27) = 14.65; p = .000

BDI Cutoffs

0-13

Minimal

14-19

Mild

20-28

Moderate

29-63

Severe

Mild -Moderate

Minimal

Slide20

Results

OQ45 Cutoffs

<63

NOT clinical

distress

>64

Clinical distress

>14 pts change

Reliable

change

Above clinical cut-off

Below clinical cut-off

Group difference

F

(2, 27) = 11.26;

p

= .000

Slide21

ResultsImaging data – no significant differences across each ROIs (ACC, Hipp., Amyg.) at baseline

 

Exp

(M,SD)

TAU

(M,SD)

C

h

(M,SD)

p-value

 

 

 

 

 

 

 

 

L ACC – L Hipp

0.19

(0.19)

0.75

(1.53)

0.12

(0.15)

0.185

L ACC – L Amyg

0.16

(0.22)

0.66

(1.42)

0.07

(0.13)

0.227

L Hipp – L Amyg

0.31

(0.12)

0.82

(1.44)

0.35

(0.19)

0.306

R ACC – R Hipp

0.20

(0.16)

0.73

(1.57)

0.15

(0.12)

0.216

R ACC – R Amyg

0.10

(0.16)

0.68

(1.44)

0.09

(0.09)

0.174

R Hipp – R Amyg

0.31

(0.07)

0.83

(1.38)

0.43

(0.16)

0.222

L ACC – R ACC

0.65

(0.15)

1.11

(1.55)

0.47

(0.15)

0.312

L Amyg – R Amyg

0.30

(0.13)

0.79

(1.41)

0.35

(0.12)

0.311

L Hipp – R Hipp

0.56

(0.13)

0.95

(1.62)

0.56

(0.13)

0.332

L ACC – R Hipp

0.15

(0.18)

0.69

(1.56)

0.13

(0.13)

0.225

L ACC – R Amyg

0.06

(0.14)

0.58

(1.47)

0.09

(0.11)

0.284

L Hipp – R ACC

0.20

(0.21)

0.77

(1.56)

0.16

(0.12)

0.190

L Hipp – R Amyg

0.25

(0.14)

0.76

(1.44)

0.29

(0.15)

0.244

L Amyg – R ACC

0.17

(0.19)

0.72

(1.42)

0.11

(0.08)

0.181

L Amyg – R Hipp

0.37

(0.10)

0.77

(1.43)

0.32

(0.13)

0.327

 

 

 

 

 

 

 

 

Slide22

Results - Follow-up

BDI Cutoffs

0-13

Minimal

14-19

Mild

20-28

Moderate

29-63

Severe

Exp: A significant decrease from moderate to minimal level

Post-hoc Tukey:

M

baseline = 24.9;

M

follow-up = 12.00;

p

-value = .0003

TAU: A shift from mild to minimal level

Post-hoc Tukey:

M

baseline = 17.7;

M

follow-up = 12.10;

p

-value = .23

Ch: Stayed at the minimal level

Post-hoc Tukey:

M

baseline = 3.70;

M

follow-up = 2.50;

p

-value = .99

Slide23

Results- Follow-up

OQ45 Cutoffs

<63

NOT clinical

distress

>64

Clinical distress

>14 pts change

Reliable

change

Exp: From above to below clinical cut-off (25 pts )

Post-hoc Tukey:

M

baseline = 84.20;

M

follow-up = 59.00

p

-value = .0002

TAU: Stayed above the clinical cut-off

Post-hoc Tukey:

M

baseline = 71.10;

M

follow-up = 63.20

p

-value = .61

Ch: Stayed below the clinical cut-off

Post-hoc Tukey:

M

baseline = 32.50;

M

follow-up = 33.60

p

-value = .99

Slide24

Results- Follow-up

Exp: A significant increase (17.39 pts)

Post-hoc Tukey:

M

baseline = 42.93;

M

follow-up = 60.33;

p

-value = .002

Ch: No significant change

Post-hoc Tukey:

M

baseline = 56.74;

M

follow-up = 56.32;

p

-value = .99

TAU: No significant change

Post-hoc Tukey:

M

baseline = 50.01;

M

follow-up = 48.51;

p

-value = .99

Slide25

Results- Follow-up

Exp: A significant increase

Post-hoc Tukey:

M

baseline = 2.74;

M

follow-up = 3.22;

p

-value = .009

TAU: No significant change

Post-hoc Tukey:

M

baseline = 2.97;

M

follow-up = 2.92;

p

-value = .99

Ch: No significant change

Post-hoc Tukey:

M

baseline = 3.15;

M

follow-up = 3.21;

p

-value = .99

Slide26

Results- Follow-up

Exp: A significant increase

Post-hoc Tukey:

M

baseline = 1.08;

M

follow-up = 1.29;

p

-value = .01

TAU: No significant change

Post-hoc Tukey:

M

baseline = 1.00;

M

follow-up = 1.03;

p

-value = .99

Ch: No significant change

Post-hoc Tukey:

M

baseline = 1.07;

M

follow-up = 1.15;

p

-value = .70

Slide27

Results- Follow-upImaging data - no significant differences across each ROIs (ACC, Hipp., Amyg.) between the two time points

Variables

 

df

MS

F

p

partial η2

L ACC – L Hipp

Time*Groups

2

0.03

0.03

0.973

0.00

L ACC – L Amyg

Time*Groups

2

0.02

0.02

0.980

0.00

L Hipp – L Amyg

Time*Groups

2

0.01

0.01

0.990

0.00

R ACC – R Hipp

Time*Groups

2

0.02

0.02

0.984

0.00

R ACC – R Amyg

Time*Groups

2

0.01

0.01

0.987

0.00

R Hipp – R Amyg

Time*Groups

2

0.08

0.07

0.933

0.00

L ACC – R ACC

Time*Groups

2

0.17

0.15

0.864

0.01

L Hipp – R Hipp

Time*Groups

2

0.11

0.08

0.921

0.00

L Amyg – R Amyg

Time*Groups

2

0.01

0.01

0.993

0.00

L ACC – R Hipp

Time*Groups

2

0.01

0.01

0.990

0.00

L ACC – R Amyg

Time*Groups

2

0.00

0.00

1.000

0.00

L Hipp – R ACC

Time*Groups

2

0.04

0.03

0.967

0.00

L Hipp – R Amyg

Time*Groups

2

0.03

0.03

0.974

0.00

L Amyg – R ACC

Time*Groups

2

0.02

0.02

1.000

0.00

L Amyg – R Hipp

Time*Groups

2

0.03

0.03

1.000

0.00

Slide28

Discussion

Main findingsExp: significant decreases in total OQ45 score (25 pts) and total BDI-II score (moderate to minimal level) between the two time pointsExp: significant increases in SDNN (17.39 pts), LF, LF/HF between the two points

Imaging data – no significant difference between groups across the two time points

Gender

Age

# of depression episodes/depression duration

Slide29

Limitations and Future DirectionsA very selected populationLongitudinal studyMaleNo active experimental condition in the control group

Comparing different psychotherapy approachesLong-term effect

Slide30

ConclusionPilot study3 comparison groupsResults only partially followed predictionsThe need for additional studies on HRV biofeedback training at different stages of depression and how it might affect participants’ neurologically.

Slide31

ReferencesAizenstein, H. J., Butters, M. A., Wu, M., Mazurkewicz, L. M., Stenger, V. A.,

Gianaros, P. J., … Carter, C. S. (2009). Altered functioning of the executive control circuit in late-life depression: Episodic and persistent phenomena. The American journal of Geriatric Psychiatry, 17, I30-42. Amr, M., El-Mogy, A., Shams, T., Vieira, K., & Lakhan, S. E. (2013). Efficacy of vitamin C as an adjunct to fluoxetine therapy in pediatric major depressive disorder: a randomized, double-blind, placebo-controlled pilot study. Nutrition Journal, 12, 1-8. Anand

, A., Li, Y., Wang, Y., Wu, J.,

Gao

, S.,

Kalnin

, A., …Lowe, M. J. (2005). Activity and connectivity of mood regulating circuit in depression: A functional magnetic resonance study.

Biological Psychiatry, 57,

1079-1088.

Beck, A. T., Steer, R. A., & Brown, G. K. (1996). Beck Depression Inventory (2

nd

ed.). San Antonio: The Psychological Corporation.

Beevers

, C. G., Ellis, A. J., & Reid, R. M. (2011). Heart rate variability predicts cognitive reactivity to sad mood provocation.

Cognitive Therapy Research, 35,

395-403.

Butler, A. C. B., Chapman, J. E., Forman, E. M.,

Beckm

, A. T. (2006). The empirical status of cognitive-behavioral therapy; a review of meta-analyses.

Clinical Psychology Review, 26,

17-31.

Campbell, S., Marriott, M.,

Nahmias

, C., &

MacQueen

, G. M. (2004). Lower hippocampal volume in patients suffering from depression: A meta-analysis.

The American Journal of Psychiatry, 161

, 598-607.

Cuijpers

, P.,

Geraedts

, A. S., van

Oppen, P., Andersson, G., Markowitz, J. C., & van

Straten

, A. (2011). Interpersonal psychotherapy of depression: a meta-analysis.

American Journal of Psychiatry, 168,

581-592.

Del

Pozo

, J. M,

Gevirtz

, R. N.,

Scher

, B., & Guarneri, E. (2004). Biofeedback treatment increases heart rate variability in patients with known coronary artery disease.

American Heart Journal, 3,

1 – 6.

Drevets

, W. C. (2001). Neuroimaging and

neuropathological

studies of depression: Implications for the cognitive-emotional features of mood disorders.

Current Opinion in Neurobiology, 11,

240-249.

Elder, B. L., &

Mosack

, V. (2011). Genetics of depression: An overview of the current science.

Issues in Mental Health Nursing, 32

, 192-202.

Gao

, S-F., & Bao, A-M. (2011). Corticotropin-releasing hormone, glutamate, and γ-aminobutyric acid in depression. The Neuroscientist, 17, 124-144. Hallman, D. M., Olsson, E. M. G., Scheele, B. V., Melin, L., & Lyskov, E. (2011). Effects of heart rate variability biofeedback in participants with stress-related chronic neck pain: A pilot study. Applied Psychophysiology and Biofeedback, 36, 71-80. Karavidas, M. K., Lehrer, P. M., Vaschillo, E., Vaschillo, B., Marin, H., Buyske, S., …, Hassett, A. (2007). Preliminary results of an open label study of heart rate variability biofeedback for the treatment of major depression. Applied Psychophysiology and Biofeedback, 32, 19 – 30. Kemp, A. H., Quintana, D. S., Felmingham, K. L., Matthews, S., & Jelinek, H. F. (2012). Depression, comorbid anxiety disorders, and heart rate variability in physically healthy, unmedicated patients: implications for cardiovascular risk. Plos One, 7, 1-8. Lehrer, P. M., Vaschillo, E., Vaschillo, B., Lu, S. E., Eckberg, D. L., Edelberg, R., … Hamer, R. M. (2003). Heart rate variability biofeedback increases baroreflex gain and peak expiratory flow. Psychosomatic Medicine, 65, 796 – 805. Lui, S., Wu, Q., Qiu, L., Yang, X., Kuang, W., Chan. R. C., …Gong, Q.(2011). Resting-state functional connectivity in treatment-resistant depression. The American Journal of Psychiatry, 168, 42-648. Mervaala, E., Fohr, J., Kononen, M., Valkonen-Korhonen, M., Vainio, P., Partanen, K., …Lehtonen, J. (2000). Quantitative MRI of the hippocampus and amygdala in severe depression. Psychological Medicine, 30, 117-125.

Oquendo

, M. A., Currier, D., & Mann, J. J. (2006). Prospective studies of suicidal behavior in major depressive and bipolar disorders: What is the evidence for predictive risk factors?

Acta

Psychiatrica

Scandinavica

, 114,

151-158.

Papakostas

, G. I. (2009). Managing partial response or nonresponse. Switching, augmentation, and combination strategies for major depressive disorder.

Journal of Clinical Psychiatry, 6,

16-25.

Patron, E.,

Benvenuti

, S. M.,

Favretto

, G.,

Valfre

, C.,

Bonfa

, C.,

Gasparotto

, R., &

Palomba

, D. (2012). Association between depression and heart rate variability in patients after cardiac surgery: A pilot study.

Journal of Psychosomatic Research, 73,

42-46.

Rush, A. J.,

Trivedi

, M H.,

Wisnieweki

, S. R.,

Nierenberq

, A. A., Stewart, J. W., Warden, D., … Fava, M. (2006). Acute and longer-term outcomes in depressed outpatients requiring one or several treatment steps: a STAR*D report.

American Journal of Psychiatry, 163,

1905-1917.

Shaffer, F., &

Venner

, J. (2013). Heart rate variability anatomy and physiology.

Biofeedback, 41,

13-25.

Sheehan, D. V.,

Lecrubier

, Y., Sheehan, K. H.,

Amorim

, P.,

Janavs

, J.,

Weiller

, E…Dunbar, G. C. (1998). The Mini-International Neuropsychiatric Interview (M.I.N.I.): The development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10.

Journal of Clinical Psychiatry, 59,

22-33.

Tonhajzerova

, I.,

Ondrejka

, I.,

Javorka

, M.,

Adamik

, P.,

Turianikova

, Z.,

Kerna

, V., …

Calkovska

, A. (2009). Respiratory sinus arrhythmia is reduced in adolescent major depressive disorder.

European Journal of Medical Research, 14,

280-283.

Waraich

, P.,

Goldner

, E. M., Somers, J. M., & Hsu, L. (2004). Prevalence and incidence studies of mood disorders: a systematic review of the literature.

Canadian Journal Psychiatry Journal, 49,

124-138.

 

Slide32

www.themegallery.com

STUDY #3 Heart Rate Variability: Biofeedback's Effect on Symptoms of Clients with Generalized Anxiety DisorderTristin Roney, Meredith Pescatello

Brigham Young University

Dissertation

Slide33

The StudyPurpose: To determine if Heart Rate Variability (HRVB) is an effective treatment for GAD 60 participants with a diagnosis of GAD Prevalence of GAD in the US ~ 2-5%CAPS clients identifying anxiety as their top concern ~20% (Winter 2016)

Heart Rate Variability: the physiological phenomenon of variation in the time interval between heartbeats. It is measured by the variation in the beat-to-beat interval.Measure of adaptability to stressLinked to several measures of health

Slide34

The Process 6 week protocolMaximize Heart Rate VariabilityDiaphragmatic Breathing Resonance Frequency Breathing Rate

Synchronization of breathing and heart rate

Slide35

How It Works

Slide36

Preliminary Results First OQTAU: 87.08HRVB: 81.90Last OQTAU: 73.39

HRVB: 56.55Mean Change TAU: -13.69 (SD=13.29)HRVB: -24.35 (SD=18.73) Total: -20.76 (SD=17.55)HRVB—treatment groupTAU—treatment as usual

Slide37

Moving Forward…Protocol consistency Lots of positive feedback from participantsMost of our participants are female Still need 10-20 more participants (especially TAU)

The importance of homework! Rationale Practice makes perfect Lasting effects?

Slide38

www.themegallery.com

STUDY #4 AAPBStress Physiology and Psychotherapy:Implementation of an HRV Biofeedback Intervention to Improve Outcome in PsychotherapyAndrea De Barros, Tara Austin, Louise WheelerDoctoral Students

Slide39

Previous Study ResultsParticipants reporting higher levels of distress (OQ > 62) had a more elevated physiological stress response and a longer physiological recovery after exposure to a stressor.

Stress reduction strategies may be a useful adjunct for those in psychotherapy ○ Particularly important for high distress groups

Slide40

GOAL & HYPOTHESES

GOAL: Assess if a HRV biofeedback intervention can help improve the psychotherapy outcome of patients with increased stress reactivityHYPOTHESES:

1. Biofeedback participants will show a significant drop in OQ

scores over time

2. Biofeedback participants will show a significantly more

elevated stress physiology at baseline

3. Biofeedback participants will show less stress physiology

at 6-week follow-up

Slide41

PARTICIPANTS

College students attending psychotherapy at university counseling center ○ Early treatment (first or second session) ○ Agreed on being contacted about research ○ Ages 18 to 30

Randomly assigned to groups

Slide42

MAIN MEASURES

Trier Social Stress Test (TSST) ○ Two stress inducing tasks ○ Gold standardOQ-45

Slide43

BIOFEEDBACK INTERVENTIONSession 1: Pre-measure of stress physiology and introduction of HRV training

○ TSST ○ Introduction of diaphragmatic breathing Session 2: Introduction of optimal rate of breathing Session 3-5: Practice of breathing at optimal rateSession 6: post-measure of stress physiology

○ TSST

Based on evidence-based protocol

(Lehrer, 2007)

Homework assignment and adherence

Slide44

CONTROL CONDITION Session 1: Pre-measure of stress physiology

○ TSST Session 2-5: passive relaxationSession 6: post-measure of stress physiology

○ TSST

Slide45

PRELIMINARY RESULTSHypothesis 1: Biofeedback participants will show a significant drop in OQ scores over time

Slide46

RESULTS Hypothesis 2:

Biofeedback participants will show a significantly more elevated stress physiology at baseline ○ Treatment group has lower SDNN, RMSSD, and HFHypothesis 3:

Biofeedback participants will show less stress physiology

at 6-week follow-up

○ Unclear because of low N but appears promising

Slide47

www.themegallery.com

STUDY #5 A Study to Determine the Efficacy of Integrating Heart Rate Variability Feedback with Psychotherapy TAULeavitt, L., Rice, M., Morrell, B.

Slide48

Qualitative study looking at the impact of HRV used in session with clientsIt is a simple process:Become trained on the use of emWave and have it installed on your computer - takes about 20 minutes.It starts in one of two waysThe client approaches you and asks about it (fliers and posters at the front desk)

If you believe it would help the client you can suggest it to them as their therapistwww.themegallery.com

Slide49

You administer the emwave HRV in session with the client, at least once.It typically takes up about 10-15 minutes of the session time, less once you have done it a few times.Once you have done one session you put the consent form in Lisa’s box with the client contact information on it.The client has a short interview about their experience and gets $15.00You have a short interview about your experience – unfortunately no $15.00 for us, we just get the satisfaction of knowing we helped out our client and a colleague!.Voila!! You are done!

www.themegallery.com

Slide50

Biofeedback Integral Part of the CAPS for 40 Years

Adjunct to therapy General stress management Referrals from physicians

Class Assignments

Increasing Demand for Services – Our Role

Most students come to 1-2 biofeedback sessions

Many psychotherapy clients tend to come for multiple sessions – individual or open hours

Provide training so students learn skills they can practice at home – breathing strategies – cutting edge treatment

Slide51

HRV – Heart Rate Variability BreathingDecrease depression

(Karavidas, et al, 2007)Decrease stress (Palomba, et al, 2011)

Improve cardiovascular functioning

(Del Pozo, Gevirtz, Scher, & Guarneri, 2004)

H/O on Breathing and Apps, Stress Cards

Stress the value of Breathing and the positive effects of HRV Breathing Training

Slide52

Paced Breathing Resources Stress CardsBreathing H/OEZ-Air PacerSmart Phone Apps

My Calm Beat Breathe2RelaxAzumio Stress DoctorInner BalanceSleep TimeSleepytimeSleepcycles Websitescalm.comasoftmurmur.comStopbreathethink.org

Slide53

What is and Why Teach and Train HRV Breathing For Autonomic Balance?Breathing is the fastest and most effective way to

calm down, reduce anxiety, attain peak performanceEmWave measures Heart Rate and Heart Rhythms Trains Autonomic Balance - balance between stress (sympathetic NS) and feeling calm (parasympathetic NS)

With slow diaphragmatic breathing HRV increases as the heart rate speeds up with inhalation and slows down with exhalation

Slide54

Biofeedback HRV Training Results

Develops Sensory Awareness of tension/anxiety vs. relaxation/calmnessAids in the Learning Process of releasing tension and stressConditions the Relaxation Response to be easy and more automatic

This results in

Greater instant calmness and mental clarity

Positive mental and emotional focus

Improved heart health over time

Peak Performance

in:

Academics

Music

Sports

Social Interactions

Slide55

Customized emWave license through the Heart Math Educational Division: Software loaded on all computers of counselors Use limited to number of sensorsAdvantagesIntegrate biofeedback with therapy Biofeedback is more effective way to teach diaphragmatic breathing

Helpful with students in crisis: Immediate skills for calmingUniversity students enjoy biofeedbackAlso in Career and Academic Success Center for student useBiofeedback for All Clinicians

Slide56

Start & Stop buttons

Various Displays

Heart Rate

Variability

Wave

Heart Rate

Scale

Breath

Pacer

Coherence

Ratio

Games and Activities

Saved Session Data

Average Heart Rate

Gray Arrow

Changes

Display

Sound on/off

emWave Main Screen

Slide57

Summary of Counseling and Psychological Services Biofeedback: Faculty and Student Dissertation Research 1. The Efficacy of Stress Management and Biofeedback Training as an Adjunct to Psychotherapy for University Students (Morrell, B., Nielsen, D., Rice, M., Erekson, D., Marvin, L., Brown, L.)

2. The Impact of Resonant Frequency HRV Training in the Treatment of Depression and Resting State fMRI (Caldwell, Y., Dissertation) 3. HRV Biofeedback’s Effect on Symptoms of Clients with Generalized Anxiety Disorder (Roney, T., Pescatello, M., Dissertation) 4. Stress Physiology and Psychotherapy: Implementation of an HRV Biofeedback intervention to improve outcome in psychotherapy (Barros, A., Austin, T., Wheeler, L. – AAPB) 5. The Efficacy of Integrating Heart Rate Variability Feedback with Psychotherapy (Leavitt, L., Rice, M., Morrell, B.)

www.themegallery.com

Slide58

Kelly

McGonigal,Ph.D

.

Make Stress Your

Friend

TED TALK

THANK YOU...