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Stress and Health Interview for Primary Care Patients With Medically Unexplained Symptoms

Stress and Health Interview for Primary Care Patients With Medically Unexplained Symptoms

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02151500
Enrollment
75
Registered
2014-05-30
Start date
2014-05-31
Completion date
2015-12-31
Last updated
2015-12-08

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

Conditions

Somatoform Disorders

Keywords

Medically Unexplained Symptoms (MUPS), Somatoform disorders, Chronic pain, Somatic symptoms, Emotional processing, Primary Care

Brief summary

The goal of this study is to test the feasibility and acceptability of providing an experiential assessment interview that targets emotional and stressful experiences in primary care. In this randomized, controlled trial, the investigators will compare an interview condition to a wait-list control condition. The investigators hypothesize that helping individuals first identify the links between their stress and symptoms will likely increase their awareness and endorsement of the link between stress and physical symptoms, including a willingness to engage in stress management techniques. It is also expected that helping raise an individual's awareness about their symptoms, followed by an experience and expression of unexpressed emotions is likely to influence their physical symptoms and psychological status.

Detailed description

Emotional stress, particularly when a patients inhibits their experiences and feelings, contributes to physical symptoms. However, primary care patients with medically unexplained symptoms are rarely assessed for the stress and emotions in an comprehensive manner. The goal of this study is to test the feasibility and acceptability of providing an experiential assessment interview that targets emotional and stressful experiences in primary care with medically unexplained physical symptoms. In this randomized, controlled trial, the investigators will compare an interview condition to a wait-list control condition. The interview will review patients health history, psychosocial history, make links between the two, and help patients identify and express emotions related to conflicts or victimization. The investigators hypothesize that helping individuals first identify the links between their stress and symptoms will likely increase their awareness and endorsement of the link between stress and physical symptoms, including a willingness to engage in stress management techniques. It is also expected that helping raise an individual's awareness about their symptoms, followed by an experience and expression of unexpressed emotions is likely to influence their physical symptoms and psychological status.

Interventions

BEHAVIORALStress and Health Interview

A stress and health interview which aims to help patients: a) disclose their stressful experiences and emotional conflicts, which might be contributing to their symptoms; b) learn about associations between their stress and physical symptoms; and c) learn about the potential value of experiencing and expressing their emotions related to these stressful situations.

Sponsors

Wayne State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Participants must score above 10 (moderate range) on the Patient Health Questionnaire-15, which is a measure of a range of medical symptoms that are often medically unexplained.

Exclusion criteria

1. Conditions that could interfere with the interview: * non-English speaking * psychosis * dementia * mental impairment 2. The presence of disease or injury that could account for the physical symptoms. - Examples: autoimmune disease, bodily injury, serious infection, cancer, heart disease, COPD, post-stroke.

Design outcomes

Primary

MeasureTime frame
Symptom Interpretation Questionnaire (SIQ)Change from baseline symptom attribution at 6-weeks

Secondary

MeasureTime frame
Brief Pain Inventory (BPI)Change from baseline pain at 6-weeks
Brief Symptom Inventory (BSI)Change from baseline symptoms at 6-weeks
Insomnia Severity Scale (ISI)Change from baseline insomnia at 6-weeks
Brief Fatigue InventoryChange from baseline fatigue at 6-weeks
Satisfaction with Life Scale (SWLS)Change from baseline life satisfaction at 6-weeks
Patient Health Questionnaire-15 (PHQ-15)Change from baseline in symptom severity at 6-weeks
Emotional Processing Scale (EPS)Change from baseline emotional processing at 6-weeks
Inventory of Interpersonal Problems Scale (IIP-32)Change from baseline interpersonal problems at 6-weeks
Pain Catastrophizing Scale (PCS)Change from baseline pain catastrophizing at 6-weeks
Change Assessment QuestionnaireChanges from baseline stage of change at 6-weeks
McGill Pain Questionnaire (SF-MPQ-2)Change from baseline pain at 6-weeks
Emotional Approach Coping Scale (EAC)Change from baseline emotional approach coping at 6-weeks

Countries

United States

Outcome results

None listed

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