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A Mobile Intervention on Values in Chronic Pain Patients.

A Mobile Intervention on Values in Chronic Pain Patients.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05205889
Enrollment
30
Registered
2022-01-25
Start date
2022-02-15
Completion date
2022-05-31
Last updated
2022-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain Syndrome

Brief summary

The study aims to test a mobile intervention on values and goals in chronic pain patients. The cognitive behavioral intervention is a 10-day course in which participants complete a brief intervention each day (about 10-20 minutes a day). The content of the intervention includes the definition of values; development of individualized values and personal value-oriented goals; and implementation of personal goals in every day life. To assess the effectiveness of the intervention, we use a multiple baseline single case design. Baseline measurements will be assessed daily between 10 and 17 days (the exact number will be randomized). Daily measurements will continue during the intervention. After the intervention, another post measurement will be collected.

Interventions

BEHAVIORALMobile intervention on values and goals in patients with chronic pain.

The protocol consists of 10 daily sessions, 10-20 Minutes each. After each session participants will complete daily measures. Participants will learn about values and a values based life. Further they will identify their own values and are encouraged to set a goal to pursue those values. Based on this, barriers to achieving goals are explained and a corresponding commitment will be made.

Sponsors

Philipps University Marburg
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

No masking is required, as participants are fully informed about the purpose of the study. Since there is only one arm, masking of the investigators is also not necessary.

Intervention model description

Single case analysis with 10-17 pre-measurement time points; 10 measurement time points during the intervention; and one post-measurement.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Chronic, non-tumor related back pain (pain for at least 6 months) * Ownership of a smartphone * Numeric Rating Scale for pain result of ≥ 4

Exclusion criteria

* High cognitive impairment (e.g., intellectual disability) * Currently in psychotherapeutic treatment * Initiation of pain-focused treatment during the study

Design outcomes

Primary

MeasureTime frameDescription
Change in Pain intensityPain intensity is assessed daily from baseline to the end of treatment (resulting in 20-27 measuring time points)Numerical Pain Rating Scale (NPRS) Minimum value: 0; Maximum value: 10 (higher scores indicate higher pain intensity)

Secondary

MeasureTime frameDescription
Change in psychological well-beingPsychological well-being is assessed daily from baseline to the end of treatment (resulting in 20-27 measuring time points)The five-item WHO Well-Being Index (WHO-5) Minimum value: 0; Maximum value 10 (range is adapted for the study; higher scores indicate higher psychological well-being)
Change in chronic pain acceptanceChronic Pain Acceptance is assessed daily from baseline to the end of the study (resulting in 20-27 measuring time points)Chronic Pain Acceptance Questionnaire (CPAQ) Minimum value: 0; Maximum value: 10 (range is adapted for the study; higher scores indicate higher pain acceptance)
Change in engaged livingEngaged Living is assessed daily from baseline to the end of the study (resulting in 20-27 measuring time points)Engaged Living Scale (ELS) Minimum value: 0; Maximum value: 10 (range is adapted for the study; higher scores indicate higher engaged living)
Change in pain catastrophizingPain Catastrophizing is assessed daily from baseline to the end of the study (resulting in 20-27 measuring time points)Pain Catastrophizing Scale (PCS) Minimum value: 0; Maximum value: 10 (range is adapted for the study; higher scores indicate higher catastrophizing)
Change in psychological flexibilityPsychological Flexibility is assessed daily from baseline to the end of the study (resulting in 20-27 measuring time points)Acceptance and Action Questionnaire 2 (AAQ-2) Minimum value: 0; Maximum value: 10 (range is adapted for the study; higher scores indicate lower psychological flexibility)
Change in self-efficacySelf-efficacy is assessed daily from baseline to the end of the study (resulting in 20-27 measuring time points)Pain Self-efficacy Questionnaire (PSEQ) Minimum value: 0; Maximum value: 10 (range is adapted for the study; higher scores indicate higher self-efficacy)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026