Completed

Peer-to-Peer Support and Psychosocial Pain Management Techniques via Facebook for Chronic Pain Patients

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Enhanced Facebook Condition

+ Control Facebook Condition

Behavioral
Who is being recruted

Neurologic Manifestations+2

+ Pain

+ Signs and Symptoms

Over 18 Years
+5 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: September 2019
See protocol details

Summary

Principal SponsorWayne State University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 27, 2019

Actual date on which the first participant was enrolled.

This study explores the benefits of a private Facebook group for people dealing with chronic pain. It's common for individuals with chronic pain to seek support from others in similar situations through social media platforms like Facebook. While there are online self-management programs available, they often lack a peer support aspect as they focus on teaching patients how to manage their pain individually. This study aims to provide a platform for peer-to-peer support and disseminate psychosocial pain management techniques using Facebook. The study involves two groups: a regular Facebook group (control group) and an enhanced Facebook group moderated by clinicians offering psychosocial pain management techniques (experimental group). The experimental group includes additional components such as pain neuroscience education, emotional validation training, guided emotional disclosure, and activities to overcome emotional and behavioral avoidance. The study's results could offer valuable insights into the impact of Facebook support groups on pain management and test if psychosocial pain interventions can be effectively shared through social media. Participants in both groups will engage in peer-to-peer healthcare and support. The experimental group will also receive psychosocial pain management techniques. The study will measure changes in pain interference and severity from the start of the study to the end of the intervention and 1-month follow-up using the Brief Pain Inventory. This inventory assesses pain interference in daily activities on a scale of 0 (does not interfere) to 10 (completely interferes). It also measures pain severity, including worst pain, average pain, and a composite of four pain items, on a scale of 0 (no pain) to 10 (pain as bad as you can imagine).

Official TitleThe Impact of Facebook Support Groups for Adults With Chronic Pain: A Randomized Clinical Trial
NCT04010019
Principal SponsorWayne State University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

119 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neurologic ManifestationsPainSigns and SymptomsPathological Conditions, Signs and SymptomsChronic Pain

Criteria

3 inclusion criteria required to participate
Must have chronic pain (i.e., pain that persists for greater than 3 months)

Must be fluent at reading and writing in English

Must have an active Facebook account and check Facebook at least 3 times a week

2 exclusion criteria prevent from participating
Terminal illness such as cancer

Active psychosis (e.g., hallucinations, delusions)

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
The enhanced Facebook group will be moderated by clinicians and offer psychosocial pain management techniques.

Group II

Active Comparator
In the control condition, there will be no outside intervention; rather, the investigators will instruct participants to offer mutual support for the duration of the group and will not comment further.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Wayne State University

Detroit, United StatesOpen Wayne State University in Google Maps
CompletedOne Study Center