Examination of Psychological and Physiological Pathways Linking Gratitude and Pain
2 other identifiers
interventional
145
1 country
1
Brief Summary
The goal of this clinical trial is to compare the effects of a brief gratitude intervention on individuals' psychological and physiological responses to acute pain. Furthermore, these associations will be examined in the context of genetic variations associated with both pain and psychological processes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 6, 2024
CompletedFirst Posted
Study publicly available on registry
March 19, 2024
CompletedStudy Start
First participant enrolled
September 10, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 19, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 19, 2025
CompletedResults Posted
Study results publicly available
April 17, 2026
CompletedApril 17, 2026
March 1, 2026
11 months
March 6, 2024
March 5, 2026
March 30, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Change in Subjective Pain Ratings From Baseline to 10-minutes Post Cold Pressor Test
Self-reported measures of pain will be reported on a numeric scale of 0 (no pain) to 10 (strongest pain imaginable every 15 seconds throughout a cold pressor test and again 1 minute and 10 minutes post cold pressor test.
Baseline to 10 minutes post cold pressor test
Differences in Pain Tolerance to Cold Pressor Test
Pain tolerance will be measured in terms of how many seconds individuals can keep their hand submerged in near-freezing water, for a maximum of up to 90 seconds (the task will be ended at that point).
Up to 1.5 minutes of Cold Pressor Test
Differences in Pain Onset to Cold Pressor Test
Pain onset will be measured in seconds between participants submerging their hands into near-freezing water and the self-reported beginning of pain.
Up to 1.5 minutes of Cold Pressor Test
Secondary Outcomes (2)
Differences in Pain-Related Cognition
Immediately after the Cold Pressor Test
Differences in Autonomic Nervous System Responsivity
Baseline to 10 minutes post cold pressor test
Study Arms (2)
Gratitude Writing
EXPERIMENTALIn the gratitude writing condition, participants will write continuously for 5 minutes about someone they are grateful for.
Neutral Writing
PLACEBO COMPARATORParticipants in the neutral writing condition will write continuously for 5 minutes about how they got to the research laboratory.
Interventions
This behavioral intervention will require participants to write about certain aspects of their lives.
Eligibility Criteria
You may qualify if:
- must be pain-free
- must be at least 18 years old
You may not qualify if:
- cardiovascular disease
- Raynaud's disease
- epilepsy
- being pregnant
- having a current injury to or open cut or sore on one's non-dominant hand
- history of fainting or seizures
- history of frostbite in non-dominant hand
- chronic pain conditions (e.g., fibromyalgia, neuropathy, arthritis)
- diabetes
- malignant tumor
- chronic lung disease
- liver disease
- kidney disease
- gastrointestinal diseases
- currently taking opioids
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Black Hills State University
Spearfish, South Dakota, 57799, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Nathan Deichert
- Organization
- Black Hills State University
Study Officials
- PRINCIPAL INVESTIGATOR
Nathan Deichert, PhD
Black Hills State University
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 6, 2024
First Posted
March 19, 2024
Study Start
September 10, 2024
Primary Completion
August 19, 2025
Study Completion
August 19, 2025
Last Updated
April 17, 2026
Results First Posted
April 17, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
All IPD that underlie results will be in a publication.