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Can Applying the Science of Habit Formation to Contemplative Practice Improve Outcomes

Can Applying the Science of Habit Formation to Contemplative Practice Improve Outcomes? A Randomized Controlled Trial of a Single-Session Habit Formation Intervention for Self-Compassionate Touch

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05866718
Enrollment
497
Registered
2023-05-19
Start date
2023-06-14
Completion date
2024-09-22
Last updated
2025-12-31

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

Conditions

Psychopathology

Keywords

Self-Compassion, Single-Session Intervention, Transdiagnostic, Intervention, Habits, Habit Formation, Micropractice, Contemplative Micropractice, Contemplative Practice, Self-Compassionate Touch, Compassion

Brief summary

In the present study, the investigators will conduct a confirmatory efficacy trial to test whether improving practice automaticity (i.e., habit formation) of self-compassionate touch improves outcomes in the predicted direction. Adults (n=440, including 20% for attrition) will be randomly assigned to: (1) the self-compassionate touch intervention plus habit formation tools (SCT+HABITS) versus (2) the self-compassionate touch intervention alone (SCT). The investigators will conduct assessments at baseline, 3-month follow-up, and 6-month follow-up. The SCT+HABITS condition will be used to evaluate whether providing habit formation tools results in superior effects to SCT. The intervention will be delivered entirely online.

Detailed description

Specific Aim 1: Evaluate whether SCT+HABITS shows more practice frequency and practice automaticity from baseline to 3-month, and to 6-month follow-up compared to the SCT. Hypothesis 1. The SCT+HABITS group will show greater increases in practice frequency and practice automaticity than SCT from baseline to 3-month, and to 6-month follow-up. Specific Aim 2: Determine whether SCT+HABITS, relative to SCT, will experience increased self-compassion and self-compassion automaticity, and reduced stress and psychopathology. Hypothesis 2. SCT+HABITS will promote greater increases in self-compassion and self-compassion automaticity, and greater reductions in stress and psychopathology from baseline to 3-month, to 6-month follow-up. Specific Aim 3: Assess whether greater baseline to 3-month follow-up increases in practice automaticity mediate the association between SCT+HABITS and baseline to 6-month follow-up increases in (a) self-compassion and (b) self-compassion automaticity, as well as reductions in (c) stress and (d) psychopathology. Hypothesis 3. Greater baseline to 3-month follow-up increases in practice automaticity will mediate the association between the SCT+HABITS group and baseline to 6-month follow-up increases in (a) self-compassion and (b) self-compassion automaticity, as well as reductions in (c) stress and (d) psychopathology. Exploratory Aim: Evaluate the barriers, facilitators, and acceptability of SCT+HABITS and SCT alone. This aim will be addressed via qualitative analyses to characterize barriers and facilitators to habit formation, and the proportion of participants in each condition (SCT+HABITS and SCT alone) who noted each type of barrier and facilitator. Participants will self-report on acceptability and feasibility via questionnaire. Then, the investigators will examine whether SCT+HABITS and SCT alone will meet or exceed the established criteria for acceptability and feasibility.

Interventions

BEHAVIORALSelf-Compassionate Touch Intervention

Participants will be taught the micropractice (\<20-second/day personal practice) via video recording.

BEHAVIORALHabit Formation Tools

Participants will receive evidence-based tools for promoting habit-formation.

Sponsors

Mind and Life Institute, Hadley, Massachusetts
CollaboratorOTHER
The Greater Good Science Center at the University of California, Berkeley
CollaboratorUNKNOWN
University of California, Berkeley
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Study participants will not be made aware that there are two experimental conditions. All will be told that they are receiving the intervention.

Intervention model description

Participants will be randomized to the SCT or SCT+HABITS using the randomizer elements in Qualtrics.

Eligibility

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

Inclusion criteria

* 18 years of age or older. * English language proficiency. * Able and willing to give informed consent. * Resides in the United States of America

Exclusion criteria

* Does not have email address or access to email. * Does not personally own a smartphone device * Not able/willing to participate in and/or complete the baseline assessments

Design outcomes

Primary

MeasureTime frameDescription
Practice FrequencyChange from baseline to 3-month follow-up, and to 6-month followupNumber of times practiced self-compassion exercise per week since last assessment. 1 item. Higher frequency indicates a better outcome.
Practice Automaticity (Practice Self-Report Behavioral Automaticity Index [SRBAI])Change from baseline to 3-month follow-up, and to 6-month follow-up.4 items, 1-9 scale. Higher scores indicate a better outcome.

Secondary

MeasureTime frameDescription
Self-Compassion Automaticity (Self-Compassion Self-Report Behavioral Automaticity Index [SRBAI])Change from baseline to 3-month follow-up, and to 6-month followup.20 items. 1-9 scale. Higher scores indicate a better outcome.
Psychopathology (DSM-5 Cross-Cutting Measure [DSM-XC])Change from baseline to 3-month follow-up, and to 6-month followup22 items (suicidality item Q11 removed). 5-point scale (0=none or not at all; 1=slight or rare, less than a day or two; 2=mild or several days; 3=moderate or more than half the days; and 4=severe or nearly every day).
Perceived Stress (Perceived-Stress Scale [PSS-10])Change from baseline to 3-month follow-up, and to 6-month followup10 items, 5 point response scale (from 0 = Never to 4 = Very Often). Lower scores indicate a better outcome. Scoring: Reverse score (e.g., 0 = 4, 1 = 3, 2 = 2, 3 = 1 & 4 = 0) items 4, 5, 7, & 8 and then summing across all scale items.
Self-Compassion (Sussex-Oxford Compassion for the Self Scale [SOCS-S])Change from baseline to 3-month follow-up, and to 6-month followup20-items, 5-point response scale. Scores can range from 20 to 100 (Higher score means higher compassion for self). Sub-scale items included.

Other

MeasureTime frameDescription
Barriers and FacilitatorsAssessed at 6-month followupThe investigators will explore first-person experience of using the practice by asking open-ended free-response questions. The investigators will develop a coding system of the barriers and facilitators to forming the habit of practicing SCT daily.
Acceptability and Feasibility (Program Feedback Scale [PFS])Assessed at 6-month followup7 Items. 5-point scale (1=really disagree; 5=totally agree)

Countries

United States

Outcome results

None listed

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