NCT06317844

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
145

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2024

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
13 days until next milestone

First Posted

Study publicly available on registry

March 19, 2024

Completed
6 months until next milestone

Study Start

First participant enrolled

September 10, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 19, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 19, 2025

Completed
8 months until next milestone

Results Posted

Study results publicly available

April 17, 2026

Completed
Last Updated

April 17, 2026

Status Verified

March 1, 2026

Enrollment Period

11 months

First QC Date

March 6, 2024

Results QC Date

March 5, 2026

Last Update Submit

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

EXPERIMENTAL

In the gratitude writing condition, participants will write continuously for 5 minutes about someone they are grateful for.

Behavioral: Behavioral Writing Intervention

Neutral Writing

PLACEBO COMPARATOR

Participants in the neutral writing condition will write continuously for 5 minutes about how they got to the research laboratory.

Behavioral: Behavioral Writing Intervention

Interventions

This behavioral intervention will require participants to write about certain aspects of their lives.

Gratitude WritingNeutral Writing

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Acute Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Results Point of Contact

Title
Nathan Deichert
Organization
Black Hills State University

Study Officials

  • Nathan Deichert, PhD

    Black Hills State University

    PRINCIPAL INVESTIGATOR

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.

Locations