---
title: Improving Activity in Adults With Chronic Pain With Online Resources
nct_id: NCT06804239
overall_status: COMPLETED
phase: NA
sponsor: Washington State University
study_type: INTERVENTIONAL
primary_condition: Chronic Pain
countries: United States
canonical_url: "https://parkinsonspathways.com/agent/trials/NCT06804239.md"
clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT06804239"
ct_last_update_post_date: 2025-09-18
last_seen_at: "2026-05-12T06:27:31.314Z"
source: ClinicalTrials.gov (mirrored, no enrichment)
---
# Improving Activity in Adults With Chronic Pain With Online Resources

**Official Title:** Improving Activity in Adults With Chronic Pain: Self-Directed Versus Guided Support With Online Resources

**NCT ID:** [NCT06804239](https://clinicaltrials.gov/study/NCT06804239)

## Key Facts

- **Status:** COMPLETED
- **Phase:** NA
- **Study Type:** INTERVENTIONAL
- **Target Enrollment:** 99
- **Lead Sponsor:** Washington State University
- **Conditions:** Chronic Pain
- **Start Date:** 2025-04-20
- **Completion Date:** 2025-08-28
- **CT.gov Last Update:** 2025-09-18

## Brief Summary

A randomized controlled study will test whether adults with chronic pain have improved outcomes when receiving a User Guide and weekly prompts for a newly designed Online Pain-Management Resource when compared to an active-control group that receives access to the Online Pain-Management Resource, but no User Guide or prompts. Outcomes of interest include measures of activity, sleep, pain and level of use of the online pain-management resource.

## Detailed Description

Participants with chronic pain will be randomized in this pilot study to an intervention group that receives a User Guide and weekly prompts to use an Online Pain-Management Resource or an active-control group that receives access to the Online Pain-Management Resource, but no User Guide or prompts. Outcomes of interest include:

i. Changes in activity and sleep over time when online resources are paired with using a wearable activity tracker (Fitbit Inspire 3®); ii. Self-reported pain and pain-related measures; and iii. Level of use of the online pain-management resource. All participants will also be asked to provide feedback on the online pain-management resource. The information collected throughout the study will inform the development team on the website's usefulness and whether guided use is superior to unguided self-directed use of the online pain resource.

## Eligibility

- **Minimum age:** 18 Years
- **Sex:** ALL
- **Healthy Volunteers:** No

```
Inclusion Criteria:

* 18 years old or older
* chronic pain at least 3 months
* interested in increasing activity level
* able to read and speak English
* reside within US
* willing to have activity tracker shipped to address
* able to download Fitbit app onto phone or computer
* willing to use Fitbit device for most days and nights during 8 weeks study

Exclusion Criteria:

* medical or psychological conditions that would prevent study participation
* planned surgery or procedure that would prevent study participation
```

## Arms

- **Intervention group** (EXPERIMENTAL) — The intervention group will receive a User Guide and weekly prompts with access to an Online Pain-Management Resource
- **Active-control** (ACTIVE_COMPARATOR) — The active-control group receives access to the Online Pain-Management Resource, but no User Guide or prompts.

## Interventions

- **User guide with prompts** (BEHAVIORAL) — A user guide and prompts to assist use of an Online Pain-Management Resource

## Primary Outcomes

- **Activity** _(time frame: 8 weeks)_ — Changes in activity as recorded on wearable activity tracker (Fitbit Inspire 3®)
- **Sleep** _(time frame: 8 weeks)_ — Changes in sleep as recorded on wearable activity tracker (Fitbit Inspire 3®)

## Secondary Outcomes

- **Pain intensity** _(time frame: 8 weeks)_
- **Pain Interference** _(time frame: 8 weeks)_
- **Chronic Pain Acceptance** _(time frame: 8 weeks)_
- **Kinesiophobia** _(time frame: 8 weeks)_
- **Sleep disturbance** _(time frame: 8 weeks)_
- **System Usability** _(time frame: 8 weeks)_
- **Client Satisfaction** _(time frame: 8 weeks)_

## Locations (2)

- Washington State University College of Nursing, Spokane, Washington, United States
- Washington State University, Spokane, Washington, United States

## Recent Field Changes (last 30 days)

- `status.overallStatus` — added _(2026-05-12)_
- `status.primaryCompletionDate` — added _(2026-05-12)_
- `status.completionDate` — added _(2026-05-12)_
- `status.lastUpdatePostDate` — added _(2026-05-12)_
- `design.phases` — added _(2026-05-12)_
- `design.enrollmentCount` — added _(2026-05-12)_
- `eligibility.criteria` — added _(2026-05-12)_
- `eligibility.minAge` — added _(2026-05-12)_
- `eligibility.sex` — added _(2026-05-12)_
- `outcomes.primary` — added _(2026-05-12)_
- `outcomes.secondary` — added _(2026-05-12)_
- `armsInterventions.arms` — added _(2026-05-12)_
- `armsInterventions.interventions` — added _(2026-05-12)_
- `sponsor.lead` — added _(2026-05-12)_
- `results.hasResults` — added _(2026-05-12)_
- `locations.washington state university college of nursing|spokane|washington|united states` — added _(2026-05-12)_
- `locations.washington state university|spokane|washington|united states` — added _(2026-05-12)_

---

*Canonical: https://parkinsonspathways.com/agent/trials/NCT06804239.md*  
*Source data (authoritative): https://clinicaltrials.gov/study/NCT06804239*  
*This page is a raw mirror with no AI summary, no editorial enrichment, and no Parkinson's-specific filtering.*