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Journeys to Wellness: A Transplant Candidate Study

Mindfulness for Symptom Reduction: A Transplant Candidate Study in Program Grant Studies of Organ Transplantation in Animals and Man 2P01 DK013083

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01254214
Enrollment
63
Registered
2010-12-06
Start date
2010-02-28
Completion date
2015-08-31
Last updated
2016-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End-stage Renal Disease

Keywords

Mindfulness, Quality of life, Transplantation, Renal disease

Brief summary

The purpose of this study is to determine whether telephone-adapted Mindfulness Based Stress Reduction (tMBSR) - a program of mindfulness meditation and gentle Hatha yoga delivered mostly by phone, is an effective program to reduce symptoms (anxiety, depression, sleep) and improve quality of life for people waiting for a kidney transplant. Participants will be randomly assigned to tMBSR or to a support group emphasizing communication skills and selecting resources. Both 8-week programs include an initial in-person meeting, 6 weekly teleconference calls, and conclude with an in-person meeting. Participants will complete questionnaires at 3 timepoints over 6 months, and if they receive a transplant, will complete additional questionnaires. Participants will complete sleep diaries and wear Actiwatches (similar to a wristwatch) for one week before programs start, and when programs end, to measure sleep. Participants will provide saliva samples, over 3 days before programs start, and again when programs end, to measure salivary cortisol, an indicator of stress. tMBSR participants will record daily home meditation practice.

Detailed description

Primary Aims 1. Test the efficacy of a telephone-adapted Mindfulness-Based Stress Reduction (tMBSR) program to reduce symptoms and improve the quality of life of kidney transplant candidates by 8-weeks and by 6-month follow-up. 2. Evaluate the impact of tMBSR on sleep measured by actigraphy, and on physiologic stress, as indicated by alteration in the slope of diurnal salivary cortisols, measured before and at the end of the 8-week active intervention period. Secondary Aims 1. Evaluate the impact of tMBSR on perceptions of transplant surgery (treatment satisfaction, pain) and of Health Related Quality of Life (HRQL) at 2-, 6- and 12-mos post-transplant surgery. 2. Design a full-scale randomized controlled trial (RCT) of the effectiveness and cost-effectiveness of tMBSR. Hypotheses * Primary: The tMBSR group will report better outcomes than an attention control support group (SG) on standardized scales for anxiety, depression, and sleep quality and health-related quality of life at 8 weeks and 6 month follow-up. * Secondary: The tMBSR group will report better outcomes than the SG group on actigraphy-derived sleep parameters and diurnal salivary cortisol patterns. * Tertiary: Candidates who attended mindfulness training will report greater treatment satisfaction, less distress from pain with transplant surgery and better HRQL 2 months, 6 months and 1 year after kidney transplantation. Rationale for study : For patients with living with kidney failure, the wait for new kidney is a stressful time. Pharmacologic therapies for managing symptoms of stress increase risks for side effects and non-adherence. Mindfulness-based stress reduction (MBSR), a non-pharmacologic program of training in mindfulness meditation, could help these patients reduce their symptom distress without increasing these other risks. Long-range Goal: To develop evidence-based recommendations for non-pharmacologic strategies that provide symptom relief to transplant patients, and are safe, practical and cost-effective. Interventions: The tMBSR program includes the curricular content of the standard 8-week MBSR program (2002 Instructor's Manual). A trained teacher provides instruction in meditation techniques including the body-scan, standing, sitting and walking meditations, and gentle Hatha yoga. Whereas the standard MBSR is conducted as 8 weekly 2.5 hour classes with a one day retreat between weeks 6 and 7, the telephone-adapted MBSR program begins with 5 hour-day workshop to introduce the techniques, followed by 6 weekly 1 ½ hour group teleconferences with the teacher to discuss the class's experiences with meditation practice, and ends with a 5 hour retreat in week 8. Home practice expectations are 25 minutes per day, 6 days a week for tMBSR. The attention control consists of two 90 minute in-person workshops and 6 1-hour teleconference calls. An experienced facilitator emphasizes communication skills and group support. Recruiting Methods: 1. Direct mail to candidates being followed by the Transplant Information Services Office with follow-up calls; invitation letters and brochures sent from the P01 Clinical Core. 2. Posters and flyers in medical clinics. 3. Referral by health providers - in- service presentations to the pre-transplant coordinators who manage the kidney candidates; 4. Additional invitations letters mailed by the coordinator who maintains the waitlist for the United Network for Organ Sharing (UNOS); study brochure or invitation letters mailed with waitlist acceptance letters. Potential Measures of intervention 'dose' or enactment: 1. Mindfulness scale: Mindful Awareness Attention Scale (MAAS); 2. Meditation practice time. Exploratory Outcomes: Post-transplant impact on Quality of Life (QOL) by Short-Form-36 item(SF-36), pain and satisfaction with transplant hospitalization. Evaluation Methods: 1. Self-report, mailed questionnaires completed at study weeks 0, 8, 26 (primary outcomes and QOL measures), 2. Actigraphy recording for 1 week prior to the intervention and during the last week of the intervention; cortisol collection for 3 days during same time periods. 3. Post transplant evaluations - 2 and 6 mos; 1 year coordinated with Transplant Database Duration of Treatment: 8 weeks Study Duration: Participants are followed up to one year post-kidney transplant. Statistical Considerations: This study is powered to compare MBSR and SG, on the primary endpoint, on the State Trait Anxiety Inventory (STAI), at 8 weeks. Randomization may be stratified by dialysis (yes/no) and history of diabetes (yes/no).

Interventions

BEHAVIORALtMBSR

MBSR is an 8-week program of mindfulness meditation and gentle Hatha yoga, taught in a class of up to 30 participants. The telephone-adapted MBSR program (tMBSR) begins with a 5 hour-day workshop to introduce the techniques, followed by 6 weekly 1 ½ hour group teleconferences with the teacher to discuss the class's experiences with meditation practice, and ends with a 5 hour retreat in week 8.

BEHAVIORALSupport group

The attention control consists of a support group emphasizing communication skills and selecting resources. It includes two 90 minute in-person workshops and 6 1-hour teleconference calls. An experienced facilitator emphasizes communication skills and group support.

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Candidate on the United Network for Organ Sharing (UNOS) wait list for a kidney or kidney-pancreas or evaluated as eligible for candidacy at the UMN * Aged 18 or older * English-speaking * Literate * Mentally intact * Able to use the telephone to participate in 6 weekly teleconferences * Able to attend 2 in-person classes in a Minnesota Metro area * Able to comply with study monitoring requirements * Receiving standard medical follow-up care * Willing to complete the informed consent process

Exclusion criteria

* Prior transplant * Medically unstable (a hospital admission for non-elective purposes in the last 3 months or major non-transplant surgery planned in the next 3 months) * Serious preexisting mental health issues: suicidality or thought disorder/psychosis; or delirium or substance abuse * Not expected to be on the waiting list \> 3 months (e.g., acceptable living donor has been identified and scheduled) * Prior MBSR class or regularly practicing mindfulness meditation (twice a week or more) * Not receiving standard medical care.

Design outcomes

Primary

MeasureTime frameDescription
State-Trait Anxiety InventoryBaseline, 8 weeks, 26 weeksThe STAI is a 20 item scale that measures current anxiety symptoms with scores that range from 20 to 80, with higher scores indicating greater levels of anxiety. The norm for working adults is a score of 34.

Secondary

MeasureTime frameDescription
Short Form -12 MCSbaseline, 8 and 26 weeksMental component summary score (MCS) of the SF-12 is a self-reported measure of mental health-related quality of life. Scores are reported as standardized T-scores, where an average (mean) score in the general population is 50 with a standard deviation of 10. Scores of 40 or less indicate impaired mental health quality or function.
SF-12 PCSbaseline, 8 weeks, 26 weeksPhysical component summary score (PCS) of the SF-12 is a self-reported measure of physical health-related quality of life.Scores are reported as standardized T-scores, where an average (mean) score in the general population is 50 with a standard deviation of 10. Scores of 40 or less indicate impaired physical health quality or function.
Pittsburgh Sleep Quality Index (PSQI)baseline, 8 weeks, 26 weeksThe PSQI is a 19-item self-reported sleep quality measure with scores that range from 0 to 21, where higher scores indicate worse sleep quality. Scores greater than 5 indicate poor sleep.
Center for Epidemiologic Studies Depression Scale (CESD)baseline, 8 weeks, 26 weeksThe CES-D is a 20-item self-report scale to measure symptoms of depression in the past week with scores having a range of 0 to 60 and a score of 16 or higher indicating clinically relevant symptoms.

Countries

United States

Participant flow

Pre-assignment details

66 people were screened, 3 were ineligible, and of the 63 who consented only 55 actually participated in the trial.

Participants by arm

ArmCount
tMBSR
telephone-adapted Mindfulness Based Stress Reduction (tMBSR) is an 8-week program of training in mindfulness meditation consisting of two in-person group meetings and 6 conference calls, led by a trained meditation teacher. tMBSR: MBSR is an 8-week program of mindfulness meditation and gentle Hatha yoga, taught in a class of up to 30 participants. The telephone-adapted MBSR program (tMBSR) begins with a 5 hour-day workshop to introduce the techniques, followed by 6 weekly 1 ½ hour group teleconferences with the teacher to discuss the class's experiences with meditation practice, and ends with a 5 hour retreat in week 8.
27
Support Group
The Support Group is a group intervention led by a trained facilitator and designed to match the intervention for time, attention and social support Support group: The attention control consists of a support group emphasizing communication skills and selecting resources. It includes two 90 minute in-person workshops and 6 1-hour teleconference calls. An experienced facilitator emphasizes communication skills and group support.
28
Total55

Baseline characteristics

CharacteristictMBSRSupport GroupTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
4 Participants5 Participants9 Participants
Age, Categorical
Between 18 and 65 years
23 Participants23 Participants46 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
1 Participants3 Participants4 Participants
Race (NIH/OMB)
Black or African American
6 Participants2 Participants8 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
1 Participants0 Participants1 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
19 Participants23 Participants42 Participants
Region of Enrollment
United States
27 participants28 participants55 participants
Sex: Female, Male
Female
19 Participants12 Participants31 Participants
Sex: Female, Male
Male
8 Participants16 Participants24 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 270 / 28
serious
Total, serious adverse events
0 / 270 / 28

Outcome results

Primary

State-Trait Anxiety Inventory

The STAI is a 20 item scale that measures current anxiety symptoms with scores that range from 20 to 80, with higher scores indicating greater levels of anxiety. The norm for working adults is a score of 34.

Time frame: Baseline, 8 weeks, 26 weeks

ArmMeasureGroupValue (MEAN)Dispersion
tMBSRState-Trait Anxiety InventoryBaseline42.1 units on a scaleStandard Deviation 12.7
tMBSRState-Trait Anxiety Inventory8 weeks40.6 units on a scaleStandard Deviation 15
tMBSRState-Trait Anxiety Inventory26 weeks41.2 units on a scaleStandard Deviation 15.3
Support GroupState-Trait Anxiety InventoryBaseline37.8 units on a scaleStandard Deviation 12.7
Support GroupState-Trait Anxiety Inventory8 weeks34.8 units on a scaleStandard Deviation 10
Support GroupState-Trait Anxiety Inventory26 weeks38.1 units on a scaleStandard Deviation 11.6
Secondary

Center for Epidemiologic Studies Depression Scale (CESD)

The CES-D is a 20-item self-report scale to measure symptoms of depression in the past week with scores having a range of 0 to 60 and a score of 16 or higher indicating clinically relevant symptoms.

Time frame: baseline, 8 weeks, 26 weeks

ArmMeasureGroupValue (MEAN)Dispersion
tMBSRCenter for Epidemiologic Studies Depression Scale (CESD)baseline15.4 units on a scaleStandard Deviation 9.9
tMBSRCenter for Epidemiologic Studies Depression Scale (CESD)8 week14.7 units on a scaleStandard Deviation 9.4
tMBSRCenter for Epidemiologic Studies Depression Scale (CESD)26 week16.9 units on a scaleStandard Deviation 11.6
Support GroupCenter for Epidemiologic Studies Depression Scale (CESD)baseline11.1 units on a scaleStandard Deviation 7.5
Support GroupCenter for Epidemiologic Studies Depression Scale (CESD)8 week9.1 units on a scaleStandard Deviation 5.8
Support GroupCenter for Epidemiologic Studies Depression Scale (CESD)26 week11.1 units on a scaleStandard Deviation 8.6
Secondary

Pittsburgh Sleep Quality Index (PSQI)

The PSQI is a 19-item self-reported sleep quality measure with scores that range from 0 to 21, where higher scores indicate worse sleep quality. Scores greater than 5 indicate poor sleep.

Time frame: baseline, 8 weeks, 26 weeks

ArmMeasureGroupValue (MEAN)Dispersion
tMBSRPittsburgh Sleep Quality Index (PSQI)baseline7.4 units on a scaleStandard Deviation 3.6
tMBSRPittsburgh Sleep Quality Index (PSQI)8 week7.3 units on a scaleStandard Deviation 4.7
tMBSRPittsburgh Sleep Quality Index (PSQI)26 week8.5 units on a scaleStandard Deviation 5.4
Support GroupPittsburgh Sleep Quality Index (PSQI)baseline6.3 units on a scaleStandard Deviation 3.7
Support GroupPittsburgh Sleep Quality Index (PSQI)8 week6.1 units on a scaleStandard Deviation 3.4
Support GroupPittsburgh Sleep Quality Index (PSQI)26 week7.1 units on a scaleStandard Deviation 4.1
Secondary

SF-12 PCS

Physical component summary score (PCS) of the SF-12 is a self-reported measure of physical health-related quality of life.Scores are reported as standardized T-scores, where an average (mean) score in the general population is 50 with a standard deviation of 10. Scores of 40 or less indicate impaired physical health quality or function.

Time frame: baseline, 8 weeks, 26 weeks

ArmMeasureGroupValue (MEAN)Dispersion
tMBSRSF-12 PCSbaseline34.5 T scoresStandard Deviation 11
tMBSRSF-12 PCS8 week38.1 T scoresStandard Deviation 10.5
tMBSRSF-12 PCS26 week33.2 T scoresStandard Deviation 9.8
Support GroupSF-12 PCSbaseline38.1 T scoresStandard Deviation 11
Support GroupSF-12 PCS8 week38.3 T scoresStandard Deviation 11.3
Support GroupSF-12 PCS26 week38.5 T scoresStandard Deviation 10.4
Secondary

Short Form -12 MCS

Mental component summary score (MCS) of the SF-12 is a self-reported measure of mental health-related quality of life. Scores are reported as standardized T-scores, where an average (mean) score in the general population is 50 with a standard deviation of 10. Scores of 40 or less indicate impaired mental health quality or function.

Time frame: baseline, 8 and 26 weeks

ArmMeasureGroupValue (MEAN)Dispersion
tMBSRShort Form -12 MCSbaseline48.9 T-ScoresStandard Deviation 8.6
tMBSRShort Form -12 MCS8 week48.3 T-ScoresStandard Deviation 8.4
tMBSRShort Form -12 MCS26 week49.7 T-ScoresStandard Deviation 9.9
Support GroupShort Form -12 MCSbaseline49.6 T-ScoresStandard Deviation 7.7
Support GroupShort Form -12 MCS8 week51.1 T-ScoresStandard Deviation 7.2
Support GroupShort Form -12 MCS26 week46.7 T-ScoresStandard Deviation 9.8

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026