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N/A N=145 Randomized Basic Science

Examination of Psychological and Physiological Pathways Linking Gratitude and Pain

Acute Pain · Positive Thinking · Emotions

Enrolled (actual)
145
Serious AEs
0.0%
Results posted
Apr 2026
Primary outcome: Primary: Change in Subjective Pain Ratings From Baseline to 10-minutes Post Cold Pressor Test — .002; .020; 3.23; 2.55 Units on a Scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Behavioral Writing Intervention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Black Hills State University
Primary completion
Aug 2025

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Subjective Pain Ratings From Baseline to 10-minutes Post Cold Pressor Test
.002; .020; 3.23; 2.55; 4.63; 3.86
PRIMARY
Differences in Pain Tolerance to Cold Pressor Test
73.310; 76.817
PRIMARY
Differences in Pain Onset to Cold Pressor Test
14.847; 18.521
SECONDARY
Differences in Pain-Related Cognition
12.457; 12.454; 9.065; 9.572
SECONDARY
Differences in Autonomic Nervous System Responsivity
86.083; 78.708; 96.388; 80.264; 95.039; 81.157

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.

Eligibility Criteria

Inclusion Criteria

  • must be pain-free
  • must be at least 18 years old

Exclusion Criteria

  • 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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06317844). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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