Summary

Eligibility
for people ages 60 years and up (full criteria)
Dates
study started
completion around

Description

Summary

The goal of this study is to better understand how two common psychological treatments for pain work in the brain of older adults living with chronic pain. This study will:

  1. evaluate fMRI of adults receiving psychological treatments for chronic pain relative to an attention control condition to determine how these interventions work within older adults, and
  2. examine self-report and EEG variables to identify for whom do these psychological interventions work.

Adults ages 60 years and older, living with chronic pain for at least 3 months will be randomly assigned to one of three conditions:

  1. Mindfulness-Meditation
  2. Self-Hypnosis
  3. Audio Recording Control

Details

Research has shown that psychological treatments can help people with chronic pain manage their pain and improve their quality of life. Two common psychological treatments for chronic pain include Mindfulness-Meditation and Self-Hypnosis. While research has shown these treatments are helpful for people with chronic pain, the benefits people experience from these types of treatments can vary from person to person. There is little research showing who responds best to which treatments and what happens in the brain during these treatments to reduce pain. The purpose of this study is to better understand how these pain treatments work in the brain. By identifying how these pain treatments work to help reduce chronic pain, the study investigators aim to improve treatments for people with chronic pain in the future.

Participants will be asked to attend 7 sessions and complete assessments in-person and online. Study sessions will consist of EEG assessment (in-person session 1), self-report measures (mixed in-person and online, all sessions), MRI and fMRI with concurrent experimental pain stimulation via heat and mechanical pain induction (in-person sessions 2 and 7) and Mindfulness-Meditation or Self-Hypnosis practice (in-person session 7 only), as well as training in Mindfulness-Meditation, Self-Hypnosis, or audio recording control (online sessions 3-6). Participants will spend about 6.5 hours in this study over a 3-week period.

Keywords

Chronic Pain, Mindfulness Meditation, Self-Hypnosis

Eligibility

You can join if…

Open to people ages 60 years and up

  1. be ≥60 years of age;
  2. have self-reported chronic pain (≥3-months, with pain experienced on ≥ 50% of days);
  3. endorse an average intensity of pain ≥3 on a 0-10 numerical rating scale (NRS) for most days of the previous 3-months;
  4. be able to read, speak, and understand English;
  5. be naïve to meditation and hypnosis (<20-min. practice/week over the past 6-months; never attended a mindfulness or self-hypnosis course); and
  6. if currently taking analgesic or psychotropic medication, medication must have been stabilized for ≥4-weeks prior to this study.

You CAN'T join if...

  1. have a history of a medical condition that could produce an abnormal EEG (e.g., epilepsy, history of traumatic brain injury);
  2. have metals in the body (e.g., clips, prosthetics, pace-makers);
  3. self-report claustrophobia or other contraindications to MRI scanning;
  4. have uncontrolled hypertension;
  5. have a primary chronic pain condition of headache;
  6. show signs of cognitive impairment (6-Item Cognitive Screener during screening; MoCA score at Session 1, using demographically-adjusted normative cut-offs that take into account race, ethnicity, and age);
  7. have chronic pain due to malignancy (e.g., cancer) or a chronic pain condition for which surgery is recommended and/or planned;
  8. are currently receiving other psychosocial treatments for any pain condition (as this may influence these treatment results);
  9. self-report previous participation in an experimental pain study; or
  10. report <2 on a 0-10 NRS for pain intensity in response to experimental "heat" pain stimuli (in order to avoid floor effects and to ensure participants are not too insensitive to thermal pain to reliably produce detectable pain-related brain activation).

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of Washington
ID
NCT06957743
Study Type
Interventional
Participants
Expecting 375 study participants
Last Updated