The primary purpose of the present study is to apply MOST methodology to determine which types of social support and mindfulness training intervention components optimally increase MVPA adoption and maintenance in Breast Cancer Survivors (BCS) in a 24-week intervention with a 48-week follow-up. The researchers will also examine the effects of changes in MVPA on symptom burden, time spent in intensities of other activities (i.e. light and sedentary), and sleep quality and duration.
Aim 1: To identify which components from four mHealth components under consideration for inclusion meaningfully contribute to improvements in MVPA at 24 and 48 weeks.
Aim 2: To examine how changes in MVPA, as a result of the 4 components, may influence additional health behaviors and outcomes including: a) symptom burden (i.e. fatigue, depression, anxiety); b) time spent i n other activity intensities (i.e. light, sedentary time); and c) sleep duration and quality.
Aim 3: To examine potential mediators (i.e. adherence, psychosocial factors such as post-traumatic growth, self-compassion, self-efficacy, and goal-setting) and moderators (i.e., age, time since diagnosis) of the four intervention components on MVPA.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
Research participant receives the Core Intervention + E-Coach + General Mindfulness Training + MVPA Specific Mindfulness Training + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
Behavioral: Buddy
Behavioral: General Mindfulness Training
Behavioral: MVPA-Specific Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 2
description
Research participant receives the Core Intervention + E-Coach + General Mindfulness Training + MVPA Specific Mindfulness Training
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
Behavioral: General Mindfulness Training
Behavioral: MVPA-Specific Mindfulness Training
Eligibility
Eligibility (as posted)
Sex
Female
Minimum age
18 Years
Show eligibility criteria text
Inclusion Criteria:
For BCS
* Female, age 18 years or older
* Stage I-III breast cancer diagnosis within the past 5 years
* Diagnosis of cancer between 18-39 years and within the past 5 years
* ≥3 months post-completion of primary treatment (i.e., surgery, chemotherapy, and/or radiation); may still be undergoing endocrine or hormone therapies
* Self-report engagement in \<60 min/week of MVPA
* Score of 0 on all positive statement(s) of the Physical Activity Readiness Questionnaire (PAR-Q)18 or willingness to obtain medical clearance from a primary care physician or oncologist
* Internet access and smartphone ownership
* Fluency in spoken and written English
* Willingness to find a buddy (someone who knows about their cancer and participation in this study and who is willing to participate by supporting them during the 24-week study), if assigned to that condition
For "Buddies"
* Friend, co-worker, caregiver or family member of a participating BCS
* Age 18 years or older
* Score of 0 on all positive statement(s) of the Physical Activity Readiness Questionnaire (PAR-Q)18 or willing to obtain medical clearance from a primary care physician
* Internet access and smartphone ownership
* Fluency in spoken and written English
* Willingness to share their Fitbit data with the study team
Exclusion Criteria:
* Absolute contraindications to exercise (i.e., acute myocardial infarction, severe orthopedic conditions), metastatic disease, or planned elective surgery
* Currently pregnant or plans to become pregnant
* Plans to move out of the United States in next 18 months
* Current enrollment in another dietary or physical activity trial
* Inability to provide informed consent
* Prisoners or other detained individuals
References
Publications (51)
BACKGROUNDMiller KD, Nogueira L, Mariotto AB, Rowland JH, Yabroff KR, Alfano CM, Jemal A, Kramer JL, Siegel RL. Cancer treatment and survivorship statistics, 2019. CA Cancer J Clin. 2019 Sep;69(5):363-385. doi: 10.3322/caac.21565. Epub 2019 Jun 11. PMID 31184787
BACKGROUNDIbrahim EM, Al-Homaidh A. Physical activity and survival after breast cancer diagnosis: meta-analysis of published studies. Med Oncol. 2011 Sep;28(3):753-65. doi: 10.1007/s12032-010-9536-x. Epub 2010 Apr 22. PMID 20411366
BACKGROUNDMcNeely ML, Campbell KL, Rowe BH, Klassen TP, Mackey JR, Courneya KS. Effects of exercise on breast cancer patients and survivors: a systematic review and meta-analysis. CMAJ. 2006 Jul 4;175(1):34-41. doi: 10.1503/cmaj.051073. PMID 16818906
BACKGROUNDSpeck RM, Courneya KS, Masse LC, Duval S, Schmitz KH. An update of controlled physical activity trials in cancer survivors: a systematic review and meta-analysis. J Cancer Surviv. 2010 Jun;4(2):87-100. doi: 10.1007/s11764-009-0110-5. Epub 2010 Jan 6. PMID 20052559
BACKGROUNDBallard-Barbash R, Friedenreich CM, Courneya KS, Siddiqi SM, McTiernan A, Alfano CM. Physical activity, biomarkers, and disease outcomes in cancer survivors: a systematic review. J Natl Cancer Inst. 2012 Jun 6;104(11):815-40. doi: 10.1093/jnci/djs207. Epub 2012 May 8. PMID 22570317
BACKGROUNDArem H, Mama SK, Duan X, Rowland JH, Bellizzi KM, Ehlers DK. Prevalence of Healthy Behaviors among Cancer Survivors in the United States: How Far Have We Come? Cancer Epidemiol Biomarkers Prev. 2020 Jun;29(6):1179-1187. doi: 10.1158/1055-9965.EPI-19-1318. Epub 2020 May 14. PMID 32409489
BACKGROUNDThraen-Borowski KM, Gennuso KP, Cadmus-Bertram L. Accelerometer-derived physical activity and sedentary time by cancer type in the United States. PLoS One. 2017 Aug 14;12(8):e0182554. doi: 10.1371/journal.pone.0182554. eCollection 2017.
type
ACTIVE_COMPARATOR
label
Exp Condition 3
description
Research participant receives the Core Intervention + E-Coach + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
Behavioral: Buddy
type
ACTIVE_COMPARATOR
label
Exp Condition 4
description
Research participant receives the Core Intervention + E-Coach
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
type
ACTIVE_COMPARATOR
label
Exp Condition 5
description
Research participant receives the Core Intervention + E-Coach + General Mindfulness Training + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
Behavioral: Buddy
Behavioral: General Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 6
description
Research participant receives the Core Intervention + E-Coach + General Mindfulness Training
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
Behavioral: General Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 7
description
Research participant receives the Core Intervention + E-Coach + MVPA Specific Mindfulness Training + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
Behavioral: Buddy
Behavioral: MVPA-Specific Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 8
description
Research participant receives the Core Intervention + E-Coach + MVPA Specific Mindfulness Training
interventionNames
Behavioral: Core Intervention
Behavioral: E-Coach
Behavioral: MVPA-Specific Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 9
description
Research participant receives the Core Intervention + General Mindfulness Training + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: Buddy
Behavioral: General Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 10
description
Research participant receives the Core Intervention + General Mindfulness Training
interventionNames
Behavioral: Core Intervention
Behavioral: General Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 11
description
Research participant receives the Core Intervention + MVPA Specific Mindfulness Training + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: Buddy
Behavioral: MVPA-Specific Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 12
description
Research participant receives the Core Intervention + MVPA Specific Mindfulness Training
interventionNames
Behavioral: Core Intervention
Behavioral: MVPA-Specific Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 13
description
Research participant receives the Core Intervention + General Mindfulness Training + MVPA Specific Mindfulness Training + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: Buddy
Behavioral: General Mindfulness Training
Behavioral: MVPA-Specific Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 14
description
Research participant receives the Core Intervention + General Mindfulness Training + MVPA Specific Mindfulness Training
interventionNames
Behavioral: Core Intervention
Behavioral: General Mindfulness Training
Behavioral: MVPA-Specific Mindfulness Training
type
ACTIVE_COMPARATOR
label
Exp Condition 15
description
Research participant receives the Core Intervention + Buddy
interventionNames
Behavioral: Core Intervention
Behavioral: Buddy
type
ACTIVE_COMPARATOR
label
Exp Condition 16
description
Research participant receives the Core Intervention
interventionNames
Behavioral: Core Intervention
Primary outcomes (1)
measure
Change in Objective Physical Activity during the 48 week technology supported physical activity interventions in breast cancer survivors
timeFrame
48 weeks
description
Physical activity will be measured at baseline, 24 and 48 weeks.The ActiGraph accelerometer will be used. At each time point, participants will wear the device for 7 consecutive days during all waking hours, except when bathing or swimming. Each valid minute of wear time will be classified according to intensity (counts/min) using commonly accepted cut-points: sedentary (\<100), light activity (100-2019) and moderate/vigorous physical activity (≥2020). Minutes of moderate and vigorous physical activity will be used to assess change.
Secondary outcomes (11)
measure
Anxiety in breast cancer survivors
timeFrame
48 weeks
description
Symptom burden of anxiety will be measured at baseline, 24 and 48 weeks using the PROMIS Item Bank v1.0 - Emotional Distress - Anxiety - Short Form 8a.
measure
Depression in breast cancer survivors
timeFrame
48 weeks
description
Symptom burden of depression will be measured at baseline, 24 and 48 weeks using the PROMIS Item Bank v1.0 - Emotional Distress - Depression-Short Form 8a.
measure
Fatigue in breast cancer survivors
timeFrame
48 weeks
description
Symptom burden of fatigue will be measured at baseline, 24 and 48 weeks using the PROMIS Item Bank v1.0 - Fatigue - Short Form 8a.
measure
Physical Function in breast cancer survivors
timeFrame
48 weeks
description
Physical function will be measured at baseline, 24 and 48 weeks using the PROMIS Item Bank v. 1.0 - Physical Function - Short Form 20a.
measure
Sleep Disturbance in breast cancer survivors
timeFrame
48 weeks
description
Symptom burden of sleep disturbance will be measured at baseline, 24 and 48 weeks using the PROMIS Item Bank v1.0 - Sleep Disturbance - Short Form 8a.
measure
Sleep Impairment in breast cancer survivors
timeFrame
48 weeks
description
Symptom burden of sleep disturbance will be measured at baseline, 24 and 48 weeks using the PROMIS Item Bank v. 1.0 - Sleep-Related Impairment - Short Form 8a.
measure
Applied Cognition Abilities in breast cancer survivors
timeFrame
48 weeks
description
Symptom burden on applied cognitive abilities will be measured at baseline, 24 and 48 weeks using the PROMIS v1.0-Applied Cognition-Abilities-Short Form 8a.
measure
Leisure Time Physical Activity in breast cancer survivors
timeFrame
48 weeks
description
Leisure time physical activity will be measured at baseline, 24 and 48 weeks using the Godin Leisure Time Exercise Questionnaire Physical Activity.
This is a measure of self-reported physical activity participation. Participants report "times per week" they participate in strenuous (e.g., jogging), moderate (e.g., fast walking), and mild (e.g., easy walking) exercise over the past 7 days and the "average duration each time you exercised (in minutes)" for each of the three activity categories. Weekly minutes of total, light, moderate, and vigorous activity are calculated by multiplying the frequency and time of each activity. This value is divided by 7 to obtain daily averages. The minimum value one can score is 0, and the maximum depends on the number of self-reported minutes of physical activity. Higher scores indicate better outcome.
measure
Light Intensity Physical Activity
timeFrame
48 weeks
description
Light intensity physical activity will be measured at baseline and at 24 and 48 weeks. The ActiGraph accelerometer will be used. At each time point, participants will wear the device for 7 consecutive days during all waking hours, except when bathing or swimming. Each valid minute of wear time will be classified according to intensity (counts/min) using commonly accepted cut-points: sedentary (\<100), light activity (100-2019) and moderate/vigorous physical activity (≥2020).
measure
Sedentary Time
timeFrame
48 weeks
description
Sedentary time will be measured at baseline and at 24 and 48 weeks. The ActiGraph accelerometer will be used. At each time point, participants will wear the device for 7 consecutive days during all waking hours, except when bathing or swimming. Each valid minute of wear time will be classified according to intensity (counts/min) using commonly accepted cut-points: sedentary (\<100), light activity (100-2019) and moderate/vigorous physical activity (≥2020).
measure
Sleep Duration
timeFrame
48 weeks
description
Sleep duration will be measured at baseline and at 24 and 48 weeks. The ActiGraph accelerometer will be used. At each time point, participants will wear the device for 7 consecutive days on their wrist while they sleep.
BACKGROUNDDevoogdt N, Van Kampen M, Geraerts I, Coremans T, Fieuws S, Lefevre J, Philippaerts R, Truijen S, Neven P, Christiaens MR. Physical activity levels after treatment for breast cancer: one-year follow-up. Breast Cancer Res Treat. 2010 Sep;123(2):417-25. doi: 10.1007/s10549-010-0997-6. Epub 2010 Jun 27. PMID 20582717
BACKGROUNDCharlier C, Van Hoof E, Pauwels E, Lechner L, Spittaels H, De Bourdeaudhuij I. The contribution of general and cancer-related variables in explaining physical activity in a breast cancer population 3 weeks to 6 months post-treatment. Psychooncology. 2013 Jan;22(1):203-11. doi: 10.1002/pon.2079. Epub 2011 Oct 5. PMID 22052746
BACKGROUNDIrwin ML, Crumley D, McTiernan A, Bernstein L, Baumgartner R, Gilliland FD, Kriska A, Ballard-Barbash R. Physical activity levels before and after a diagnosis of breast carcinoma: the Health, Eating, Activity, and Lifestyle (HEAL) study. Cancer. 2003 Apr 1;97(7):1746-57. doi: 10.1002/cncr.11227. PMID 12655532
BACKGROUNDPhillips SM, McAuley E. Social cognitive influences on physical activity participation in long-term breast cancer survivors. Psychooncology. 2013 Apr;22(4):783-91. doi: 10.1002/pon.3074. Epub 2012 Mar 26. PMID 22451113
BACKGROUNDThorsen L, Courneya KS, Stevinson C, Fossa SD. A systematic review of physical activity in prostate cancer survivors: outcomes, prevalence, and determinants. Support Care Cancer. 2008 Sep;16(9):987-97. doi: 10.1007/s00520-008-0411-7. Epub 2008 Feb 15. PMID 18274783
BACKGROUNDStevinson C, Tonkin K, Capstick V, Schepansky A, Ladha AB, Valance JK, Faught W, Steed H, Courneya KS. A population-based study of the determinants of physical activity in ovarian cancer survivors. J Phys Act Health. 2009 May;6(3):339-46. doi: 10.1123/jpah.6.3.339. PMID 19564663
BACKGROUNDKampshoff CS, Jansen F, van Mechelen W, May AM, Brug J, Chinapaw MJ, Buffart LM. Determinants of exercise adherence and maintenance among cancer survivors: a systematic review. Int J Behav Nutr Phys Act. 2014 Jul 2;11:80. doi: 10.1186/1479-5868-11-80. PMID 24989069
BACKGROUNDValle CG, Tate DF. Engagement of young adult cancer survivors within a Facebook-based physical activity intervention. Transl Behav Med. 2017 Dec;7(4):667-679. doi: 10.1007/s13142-017-0483-3. PMID 28374211
BACKGROUNDSchneider J, Malinowski P, Watson PM, Lattimore P. The role of mindfulness in physical activity: a systematic review. Obes Rev. 2019 Mar;20(3):448-463. doi: 10.1111/obr.12795. Epub 2018 Nov 23. PMID 30468299
BACKGROUNDRabin C, Pinto B, Fava J. Randomized Trial of a Physical Activity and Meditation Intervention for Young Adult Cancer Survivors. J Adolesc Young Adult Oncol. 2016 Mar;5(1):41-7. doi: 10.1089/jayao.2015.0033. Epub 2015 Oct 15. PMID 26812450
BACKGROUNDCourneya KS, Rogers LQ, Campbell KL, Vallance JK, Friedenreich CM. Top 10 research questions related to physical activity and cancer survivorship. Res Q Exerc Sport. 2015 Jun;86(2):107-16. doi: 10.1080/02701367.2015.991265. Epub 2015 Jan 28. PMID 25629322
BACKGROUNDHedeker D, Gibbons RD, Waternaux C. Sample size estimation for longitudinal designs with attrition: comparing time-related contrasts between two groups. Journal of Educational and Behavioral Statistics. 1999;24(1):70-93.
BACKGROUNDBuchholz SW, Wilbur J, Ingram D, Fogg L. Physical activity text messaging interventions in adults: a systematic review. Worldviews Evid Based Nurs. 2013 Aug;10(3):163-73. doi: 10.1111/wvn.12002. Epub 2013 Jun 7. PMID 23746267
BACKGROUNDFreedson PS, Melanson E, Sirard J. Calibration of the Computer Science and Applications, Inc. accelerometer. Med Sci Sports Exerc. 1998 May;30(5):777-81. doi: 10.1097/00005768-199805000-00021. PMID 9588623
BACKGROUNDWelk GJ, McClain JJ, Eisenmann JC, Wickel EE. Field validation of the MTI Actigraph and BodyMedia armband monitor using the IDEEA monitor. Obesity (Silver Spring). 2007 Apr;15(4):918-28. doi: 10.1038/oby.2007.624. PMID 17426327
BACKGROUNDCampbell KL, Winters-Stone KM, Wiskemann J, May AM, Schwartz AL, Courneya KS, Zucker DS, Matthews CE, Ligibel JA, Gerber LH, Morris GS, Patel AV, Hue TF, Perna FM, Schmitz KH. Exercise Guidelines for Cancer Survivors: Consensus Statement from International Multidisciplinary Roundtable. Med Sci Sports Exerc. 2019 Nov;51(11):2375-2390. doi: 10.1249/MSS.0000000000002116. PMID 31626055
BACKGROUNDGodin G, Shephard RJ. A simple method to assess exercise behavior in the community. Can J Appl Sport Sci. 1985 Sep;10(3):141-6. PMID 4053261
BACKGROUNDGarcia SF, Cella D, Clauser SB, Flynn KE, Lad T, Lai JS, Reeve BB, Smith AW, Stone AA, Weinfurt K. Standardizing patient-reported outcomes assessment in cancer clinical trials: a patient-reported outcomes measurement information system initiative. J Clin Oncol. 2007 Nov 10;25(32):5106-12. doi: 10.1200/JCO.2007.12.2341. PMID 17991929
BACKGROUNDPilkonis PA, Choi SW, Reise SP, Stover AM, Riley WT, Cella D; PROMIS Cooperative Group. Item banks for measuring emotional distress from the Patient-Reported Outcomes Measurement Information System (PROMIS(R)): depression, anxiety, and anger. Assessment. 2011 Sep;18(3):263-83. doi: 10.1177/1073191111411667. Epub 2011 Jun 21. PMID 21697139
BACKGROUNDLai J-S, Cella D, Choi S, Teresi JA, Hays RD, Stone AA. Developing a fatigue item bank for the Patient-Reported Outcomes Measurement Information System (PROMIS FIB version 1). Presented at the Meeting of the Survey Methods in Multicultural, Multinational, and Multiregional Contexts (3MC), Berlin, Germany. 2008.
BACKGROUNDBuysse DJ, Yu L, Moul DE, Germain A, Stover A, Dodds NE, Johnston KL, Shablesky-Cade MA, Pilkonis PA. Development and validation of patient-reported outcome measures for sleep disturbance and sleep-related impairments. Sleep. 2010 Jun;33(6):781-92. doi: 10.1093/sleep/33.6.781. PMID 20550019
BACKGROUNDChadwick P, Hember M, Symes J, Peters E, Kuipers E, Dagnan D. Responding mindfully to unpleasant thoughts and images: reliability and validity of the Southampton mindfulness questionnaire (SMQ). Br J Clin Psychol. 2008 Nov;47(Pt 4):451-5. doi: 10.1348/014466508X314891. Epub 2008 Jun 20. PMID 18573227
BACKGROUNDRaes F, Pommier E, Neff KD, Van Gucht D. Construction and factorial validation of a short form of the Self-Compassion Scale. Clin Psychol Psychother. 2011 May-Jun;18(3):250-5. doi: 10.1002/cpp.702. Epub 2010 Jun 8. PMID 21584907
BACKGROUNDTedeschi RG, Calhoun LG. The Posttraumatic Growth Inventory: measuring the positive legacy of trauma. J Trauma Stress. 1996 Jul;9(3):455-71. doi: 10.1007/BF02103658. PMID 8827649
BACKGROUNDMcAuley E. Self-efficacy and the maintenance of exercise participation in older adults. J Behav Med. 1993 Feb;16(1):103-13. doi: 10.1007/BF00844757. PMID 8433355
BACKGROUNDWojcicki TR, White SM, McAuley E. Assessing outcome expectations in older adults: the multidimensional outcome expectations for exercise scale. J Gerontol B Psychol Sci Soc Sci. 2009 Jan;64(1):33-40. doi: 10.1093/geronb/gbn032. Epub 2009 Jan 29. PMID 19181688
BACKGROUNDRovniak LS, Anderson ES, Winett RA, Stephens RS. Social cognitive determinants of physical activity in young adults: a prospective structural equation analysis. Ann Behav Med. 2002 Spring;24(2):149-56. doi: 10.1207/S15324796ABM2402_12. PMID 12054320
BACKGROUNDSallis JF, Grossman RM, Pinski RB, Patterson TL, Nader PR. The development of scales to measure social support for diet and exercise behaviors. Prev Med. 1987 Nov;16(6):825-36. doi: 10.1016/0091-7435(87)90022-3. PMID 3432232
BACKGROUNDRosenberg, M. Society and the adolescent self-image. Princeton, NJ: Princeton University Press.1965.
BACKGROUNDFox, K.R., & Corbin, C.B. The physical self-perception profile: Development and preliminary validation. Journal of Sport & Exercise Psychology, 11, 408-430 1989.
BACKGROUNDKendzierski D, DeCarlo KJ. Physical Activity Enjoyment Scale: Two validation studies. Journal of Sport & Exercise Psychology. 1991.
BACKGROUNDCollins LM, Baker TB, Mermelstein RJ, Piper ME, Jorenby DE, Smith SS, Christiansen BA, Schlam TR, Cook JW, Fiore MC. The multiphase optimization strategy for engineering effective tobacco use interventions. Ann Behav Med. 2011 Apr;41(2):208-26. doi: 10.1007/s12160-010-9253-x. PMID 21132416
BACKGROUNDCollins LM, Murphy SA, Nair VN, Strecher VJ. A strategy for optimizing and evaluating behavioral interventions. Ann Behav Med. 2005 Aug;30(1):65-73. doi: 10.1207/s15324796abm3001_8. PMID 16097907
BACKGROUNDPinheiro JC, Bates DM. Approximations to the log-likelihood function in the nonlinear mixed-effects model. Journal of Computational and Graphical Statistics. 1995;4(1):12-35.
BACKGROUNDKrull JL, MacKinnon DP. Multilevel Modeling of Individual and Group Level Mediated Effects. Multivariate Behav Res. 2001 Apr 1;36(2):249-77. doi: 10.1207/S15327906MBR3602_06. PMID 26822111
BACKGROUNDDiCiccio TJ, Efron B. Bootstrap confidence intervals. Statistical science. 1996:189-212.
BACKGROUNDHankin VV, D.; Polster, R. . Maximizing Acceptance and Enrollment in MBSR Randomized Controlled Trials with Older Men Diagnosed with Cancer. . Poster presented to the 8th Annual International Scientific Conference of Mindfulness in Medicine, Health Care, and Society Worcester, MA. 2010.
BACKGROUNDVictorson D, Du H, Hankin V, et al. Mindfulness-based stress reduction decreases fear of progression over time for men with prostate cancer on active surveillance: results from a randomized clinical trial. J Urol. 2012;187(4S):384.
BACKGROUNDVictorson D, Hankin V, Burns J, Weiland R, Maletich C, Sufrin N, Schuette S, Gutierrez B, Brendler C. Feasibility, acceptability and preliminary psychological benefits of mindfulness meditation training in a sample of men diagnosed with prostate cancer on active surveillance: results from a randomized controlled pilot trial. Psychooncology. 2017 Aug;26(8):1155-1163. doi: 10.1002/pon.4135. Epub 2016 May 3. PMID 27145355
BACKGROUNDVictorson D, Maletich C, Gutierrez B, Schuette S, Morgan T, Kutikov A, Kundu S, Eggener S, Brendler C. Description of a new national cancer institute funded randomized controlled trial
BACKGROUNDVictorson D, Garland, E, Hanley, A, Greco, C. Is mindfulness immeasurable? Discovery and dialogue of conceptual, practical, scientific, and experiential solutions. Glob Adv Health Med. 2018 7(1160):13.
BACKGROUNDVictorson D, Maletich, C, Sufrin, N, Schuette, S, Gutierrez, B, Cordero, E, Johnson, C, Stencel, D, Bakosh, L, Ring, M. Development of a New Clinical Mindfulness Research Tool to Enhance, Deliver and Streamline Online Mindfulness Interventions. J Altern Complement Med. 2016;0(0):A21.
DERIVEDWolter M, Reading JM, Solk P, Starikovsky J, Hasanaj K, Wang SD, Siddique J, Horowitz B, Spring B, Carden LB, Fox R, Sauer C, Freeman H, Frey J, Victorson D, Phillips SM. Optimizing a mHealth physical activity intervention with mindful awareness lessons in breast cancer survivors: Fit2ThriveMIND protocol. Contemp Clin Trials. 2025 Sep;156:108038. doi: 10.1016/j.cct.2025.108038. Epub 2025 Jul 31. PMID 40752821