Chronic PainASI-SRNCT04998734
Validation of the ASI-SR Form in a Population of Chronic Non-cancer Pain Patients
An observational study of Chronic Pain and Opioid-use Disorder, run by Uppsala University at 1 site in Sweden.
Trial summary
The Swedish version of ASI-SR has shown good feasibility in assessment of addiction patients functioning compare to long and time-consuming ASI, which is upp to date golden standard in Sweden. This study investigate if ASI-SR is suitable instrument for the assessment of the chronic pain patient addicted to opioids. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Chronic Pain, Opioid-use Disorder, Quality of Life
- What is being tested?
- ASI-SR
- How many people
- 1 participants
- Where
- 1 siteSweden
- Study dates
- 5 Aug 2021to 28 Mar 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: In this days there are approx. 100 patients treated in the substitution program, 1300 patients receiving referral to the pain clinic in Uppsala Pain Center.
Who may be able to join
- Chronic non-cancer related pain
- ongoing treatment in the clinic
Who cannot join
- severe cognitive impairment
- illiterate in Swedish
- inability to give informed consent.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: ASI-SR Form as a Standardized Instrument for Healthcare Management of Chronic Non-cancer Pain Patients
The Swedish version of ASI-SR has shown good feasibility in assessment of addiction patients functioning compare to long and time-consuming ASI, which is upp to date golden standard in Sweden. This study investigate if ASI-SR is suitable instrument for the assessment of the chronic pain patient addicted to opioids. The validation process is designed according to the COSMIN guidelines.
Preliminary results are expected by December 2022.
Read the detailed description
The use of opioids in treatment of chronic non- cancer pain (CNCP) has increased during the past decades in most parts of the western world. Use of prescription opioids can lead to problematic opioid use which can be life-threatening with significant morbidity and mortality. Studies have found that 21-29% of CNCP patients receiving chronic opioid therapy (COT) ( receiving opioids for > 90 days) have problematic opioid use. Individuals with chronic pain and co-occurring substance use disorders and/or mental health disorders, have increased risk for problematic use of prescribed opioids.
Several screening instruments and strategies have been introduced in recent years for identifying patients not suitable for opioid therapy. Even so, there is no single test or instrument that can reliably identify those patients at risk for developing problematic opioid use or opioid use disorder if opioid therapy is initiated, or identify those who need increased monitoring during treatment.
Addiction Severity Index (ASI) is a standardized semi-structured interview used for assessing severity and need of treatment in seven functional domains associated to substance use disorders; physical health, employment/support status, alcohol use, drug use, legal status, family/social functioning and psychiatric health. The ASI was developed in the US. by McLellan and colleagues and is widely used all over the world, both in research and for clinical assessment and treatment evaluations . The ASI could be a useful instrument for a multidimensional assessment of patients with chronic non-cancer where opioid treatment is considered, and it could also be used for evaluation of ongoing opioid therapy . However, the ASI interview is a time consuming instrument. To conduct an interview takes between 45-60 minutes and is followed by 20-25 minutes of administrative work. In the year of 2000 Rosen et al tested a short self-report form based the items used to calculate the ASI composite scores that asses current function and problem severity. This questionnaire was translated by our research group and tested on a sample of individuals referred to the Addiction clinic at Uppsala University Hospital. The study suggested that a self-administered questionnaire based on the subscales of the ASI composite scores is a feasible alternative to the ASI interview for assessing patient functioning in the different domains and screen for current problematic alcohol- or drug use .
A validated screening tool that provides both an effective method of assessing patients and identifying problems in several different life domains, and identify substance use related problems if they should arise, would be beneficial in clinical practice when deciding what treatment to offer. Such an instrument could potentially decrease the risk of iatrogenic opioid use disorder.
Purpose and aims The main objective with this study is to test the psychometric properties of the ASI-SR in a population of CNCP patients. 'Secondary aim is to describe differences between subjects treated within the substitution therapy program and those who are treated within the pain clinic.
Method:
Sample Participants for this study will be recruited from outpatient pain clinic and addiction clinic at Uppsala University Hospital, and Linköping University Hospital Sweden. Eligible for participation are persons >18-65 years of age with current CNCP and ongoing treatment at the facilities. Estimated number of participant needed is about 200.
Exclusion criteria are severe cognitive impairment, illiterate in Swedish, and inability to give informed consent.
Procedures Eligible participants will be approached and asked if they can consider to participate in the study by clinical staff at the facilities. If they accept, they will receive an e-mail with a link to the questionnaires and to written information about the study. If they decide to participate they will give informed consent by signing a digital consent form. A digital battery of questionnaires containing the ASI-SR and a validity battery will then be provided to the participants to fill out. The validity battery will consist of self-report forms. To participants that do not respond to the questionnaires and have not declined participation, reminders will be sent out by text-messages, e-mail and mail. Four days after the participants have completed the questionnaires they will receive an e-mail with a link the ASI-SR form to fill out once more to test re-test reliability.
Participants that do not want to or do not have access to the digitalized versions of the questionnaires will be offered to fill out paper versions of the questionnaires sent to them by mail.
Measures ASI-SR is a 38 question self-administered form based on the items used to calculate the ASI's composite scores, measuring current problems and severity in seven domains . The CS ranges from 0 to 1 where 0 indicates no problems.
The validity battery consist of self-administered questionnaires that correspond to six out of seven of the ASI-SR's domains. These questionnaires will be used as concurrent validity measures for all the ASI-SR composite scores (CS) except the CS for legal situation. The participants will fill out questions about current pain intensity and pain interference, the Rand 36 for multidimensional health related quality of life , pain related disability Pain Disability Index (PDI) and Sheehan Disability Scale (SDS) which measures disability across domains of work/school, social life, and family life/home responsibilities . The Alcohol Use Disorder Identification Test (AUDIT) will be used for assessment of problematic alcohol use and the Drug Use Disorder Identification Test (DUDIT) for assessment of problematic illicit drug use . PHQ9 will assess depressive symptoms and the GAD 7 will be used for assessment of anxiety symptoms . Patient global impression of change (P-GIC) will be used to evaluate if the participants experienced any changes in global health between test-retest of the ASI-SR. P-GIC is gold standard for measuring change in CNCP patients .
Statistics Statistical analyses will be done using SPSS (Version 23, IBM SPSS Statistics for Windows, Armonk, NY: IBM Corp). Calculation of the CS follow standard procedure . Consistency of CS between the interview and the self-report will be evaluated on the individual basis by interclass correlation analysis (ICC) and at group level with paired t-test or Wilcoxon signed rank test if data is not normally distributed. ICC coefficient is considered to be poor if it is less than 0.40, fair between 0.40-0.59 , good between 0.60-0.70 and excellent between 0.75-1.00 .
Reliability and internal consistency will be evaluated using Cronbach's α. The α coefficient is considered acceptable if it is above 0.70 .
The concurrent validity of each score will be assessed with suitable correlation analyses between the ASI-SR composite score(s) and the external validity measure(s).
To assess discriminant validity of the ASI-SR composite scores and external validity measures, an intercorrelation matrix between ASI-SR composite scores, and composite scores and external measures will be computed.
For evaluating factor structure principal component analyses (PCA) will be used.
Relevance for the field Opioid therapy for chronic non-cancer pain has emerged as a problematic treatment and the evidence is scarce for its effectiveness . However, there are some individuals that seem to benefit from opioid therapy and most guidelines propose an individual approach to management, beginning with a comprehensive patient evaluation, focusing on factors that may indicate potential substance use disorder. When opioids are used, clinicians should closely monitor patients for loss of response, adverse effects or aberrant behavior, and assess treatment outcome . There is a need for a multi-dimensional instrument that can assess problems related to increased risk for developing problematic opioid use, i.e. opioid use disorder, psychiatric co-morbidity and social problems. The ASI-SR could be an effective way of screening for current problems in different life domains and to monitor and evaluate ongoing treatment and identify problems if they would arise. Additional measures include urine or saliva drug testing, prescription practice, opioid treatment agreements, and universal precautions in conjunction with opioid therapy.
Ethical considerations The study will be sent to the Regional Ethical Review Board in Uppsala. Participants will be anonymous and all data will be coded before processed.
- Being tested
- ASI-SR
- Keywords
- opioids, ASI-SR, pain, opioid-use disorder, dependence, validation, assessment
- Medical subject headings
- Chronic Pain, Opioid-Related Disorders, Risk Reduction Behavior, Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ASI-SRDiagnostic test
Psychometric properties of ASI-SR
| Study group | Role | What they receive |
|---|---|---|
| Chronic pain | Patients with chronic non-cancer pain referred to secondary and tertiary care Receives: Diagnostic Test: ASI-SR |
What is being measured
The primary outcome is the main question the study is designed to answer.
Addiction Severity Index - Short version
The main objective with this study is to test the psychometric properties of the ASI-SR in a population of CNCP patients.Consistency of CS between the interview and the self-report will be evaluated on the individual basis by interclass correlation analysis (ICC) and at group level with paired t-test or Wilcoxon signed rank test if data is not normally distributed. ICC coefficient is considered to be poor if it is less than 0.40, fair between 0.40-0.59 , good between 0.60-0.70 and excellent between 0.75-1.00.
Measured: Baseline
Secondary outcomes (8)
Patient Global Impression of Change
7-grade scale (-3-+3)where the lowest points indicate negative and highest points indicate positive change.
Measured: Baseline
Addiction Severity Index -Short version
Second test ASI-SR for reproducibility( 0,1 answer /scores in different categories)
Measured: 4-7 days later
Generalised Anxiety Disorder 7
Generalised Anxiety Disorder 7-item scale (0-21) The higher the score the higher severity of the anxiety disorder, cut-off 10.
Measured: baseline
Research and Development 36-Item Health Survey RAND-36
Quality of life instrument of International Resource Center for Health Care considering both physical and mental health aspects. Scores 0-100. The Higher score the better quality of life in different segments of well-being, function or quality of life.
Measured: Baseline
Pain Disability Index
7-question score system for different pain groups,(0-70). The higher the index the greater the persons disability due to the pain.
Measured: Baseline
Alcohol Use Disorder Identification Test
Scoring system, (0-40)where increase of the points reflects increased risk of problematic alcohol use.
Measured: Baseline
Drug Use Disorder Identification Test
Scoring system,(0-44) where increase of the points reflects increased probability of drug abuse syndrome.
Measured: Baseline
Patient Health Questionnaire PHQ9
Depression Assesment scoring system, (0-15) where <4 is no need of depression treatment, and >15 identifies need of pharmacologic or other depression treatment
Measured: Baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Aug 2021
- Study start5 Aug 2021
- Primary completion1 Jun 2022
- Study completion28 Mar 2023
Why it stopped: Recruitment failure
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic PainStudies of the same condition, open and under way.
- More trials run by Uppsala UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 1 participants (actual)
Sponsor and investigators
- Lead sponsor
- Uppsala University
- Sponsor type
- University, hospital or other
- Collaborators
- Uppsala University Hospital
- Responsible party
- Sponsor
- Investigators
- Pernilla Åsenlöf, Profesor, Principal investigator, Uppsala University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04998734
- Sponsor's protocol ID
- 2020-001-5
- Acronym
- ASI-SR
- Status last verified
- May 2023
- First submitted
- 2 Aug 2021
- Last updated
- 11 May 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- ASI-SR Form as a Standardized Instrument for Healthcare Management of Chronic Non-cancer Pain Patients
- ClinicalTrials.gov ID
- NCT04998734
- Acronym / sponsor ID
- ASI-SR / 2020-001-5
- Keywords
- opioids, ASI-SR, pain, opioid-use disorder, dependence, validation, assessment
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: Recruitment failure
- Enrolment
- 1 participants (actual)
- Lead sponsor
- Uppsala UniversityUniversity, hospital or other
- Collaborators
- Uppsala University Hospital
- Study start
- 5 Aug 2021 (actual)
- Primary completion
- 1 Jun 2022 (actual)
- Study completion
- 28 Mar 2023 (actual)
- First posted
- 10 Aug 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The Swedish version of ASI-SR has shown good feasibility in assessment of addiction patients functioning compare to long and time-consuming ASI, which is upp to date golden standard in Sweden. This study investigate if ASI-SR is suitable instrument for the assessment of the chronic pain patient addicted to opioids. The validation process is designed according to the COSMIN guidelines.
Preliminary results are expected by December 2022.
Detailed description
The use of opioids in treatment of chronic non- cancer pain (CNCP) has increased during the past decades in most parts of the western world. Use of prescription opioids can lead to problematic opioid use which can be life-threatening with significant morbidity and mortality. Studies have found that 21-29% of CNCP patients receiving chronic opioid therapy (COT) ( receiving opioids for > 90 days) have problematic opioid use. Individuals with chronic pain and co-occurring substance use disorders and/or mental health disorders, have increased risk for problematic use of prescribed opioids.
Several screening instruments and strategies have been introduced in recent years for identifying patients not suitable for opioid therapy. Even so, there is no single test or instrument that can reliably identify those patients at risk for developing problematic opioid use or opioid use disorder if opioid therapy is initiated, or identify those who need increased monitoring during treatment.
Addiction Severity Index (ASI) is a standardized semi-structured interview used for assessing severity and need of treatment in seven functional domains associated to substance use disorders; physical health, employment/support status, alcohol use, drug use, legal status, family/social functioning and psychiatric health. The ASI was developed in the US. by McLellan and colleagues and is widely used all over the world, both in research and for clinical assessment and treatment evaluations . The ASI could be a useful instrument for a multidimensional assessment of patients with chronic non-cancer where opioid treatment is considered, and it could also be used for evaluation of ongoing opioid therapy . However, the ASI interview is a time consuming instrument. To conduct an interview takes between 45-60 minutes and is followed by 20-25 minutes of administrative work. In the year of 2000 Rosen et al tested a short self-report form based the items used to calculate the ASI composite scores that asses current function and problem severity. This questionnaire was translated by our research group and tested on a sample of individuals referred to the Addiction clinic at Uppsala University Hospital. The study suggested that a self-administered questionnaire based on the subscales of the ASI composite scores is a feasible alternative to the ASI interview for assessing patient functioning in the different domains and screen for current problematic alcohol- or drug use .
A validated screening tool that provides both an effective method of assessing patients and identifying problems in several different life domains, and identify substance use related problems if they should arise, would be beneficial in clinical practice when deciding what treatment to offer. Such an instrument could potentially decrease the risk of iatrogenic opioid use disorder.
Purpose and aims The main objective with this study is to test the psychometric properties of the ASI-SR in a population of CNCP patients. 'Secondary aim is to describe differences between subjects treated within the substitution therapy program and those who are treated within the pain clinic.
Method:
Sample Participants for this study will be recruited from outpatient pain clinic and addiction clinic at Uppsala University Hospital, and Linköping University Hospital Sweden. Eligible for participation are persons >18-65 years of age with current CNCP and ongoing treatment at the facilities. Estimated number of participant needed is about 200.
Exclusion criteria are severe cognitive impairment, illiterate in Swedish, and inability to give informed consent.
Procedures Eligible participants will be approached and asked if they can consider to participate in the study by clinical staff at the facilities. If they accept, they will receive an e-mail with a link to the questionnaires and to written information about the study. If they decide to participate they will give informed consent by signing a digital consent form. A digital battery of questionnaires containing the ASI-SR and a validity battery will then be provided to the participants to fill out. The validity battery will consist of self-report forms. To participants that do not respond to the questionnaires and have not declined participation, reminders will be sent out by text-messages, e-mail and mail. Four days after the participants have completed the questionnaires they will receive an e-mail with a link the ASI-SR form to fill out once more to test re-test reliability.
Participants that do not want to or do not have access to the digitalized versions of the questionnaires will be offered to fill out paper versions of the questionnaires sent to them by mail.
Measures ASI-SR is a 38 question self-administered form based on the items used to calculate the ASI's composite scores, measuring current problems and severity in seven domains . The CS ranges from 0 to 1 where 0 indicates no problems.
The validity battery consist of self-administered questionnaires that correspond to six out of seven of the ASI-SR's domains. These questionnaires will be used as concurrent validity measures for all the ASI-SR composite scores (CS) except the CS for legal situation. The participants will fill out questions about current pain intensity and pain interference, the Rand 36 for multidimensional health related quality of life , pain related disability Pain Disability Index (PDI) and Sheehan Disability Scale (SDS) which measures disability across domains of work/school, social life, and family life/home responsibilities . The Alcohol Use Disorder Identification Test (AUDIT) will be used for assessment of problematic alcohol use and the Drug Use Disorder Identification Test (DUDIT) for assessment of problematic illicit drug use . PHQ9 will assess depressive symptoms and the GAD 7 will be used for assessment of anxiety symptoms . Patient global impression of change (P-GIC) will be used to evaluate if the participants experienced any changes in global health between test-retest of the ASI-SR. P-GIC is gold standard for measuring change in CNCP patients .
Statistics Statistical analyses will be done using SPSS (Version 23, IBM SPSS Statistics for Windows, Armonk, NY: IBM Corp). Calculation of the CS follow standard procedure . Consistency of CS between the interview and the self-report will be evaluated on the individual basis by interclass correlation analysis (ICC) and at group level with paired t-test or Wilcoxon signed rank test if data is not normally distributed. ICC coefficient is considered to be poor if it is less than 0.40, fair between 0.40-0.59 , good between 0.60-0.70 and excellent between 0.75-1.00 .
Reliability and internal consistency will be evaluated using Cronbach's α. The α coefficient is considered acceptable if it is above 0.70 .
The concurrent validity of each score will be assessed with suitable correlation analyses between the ASI-SR composite score(s) and the external validity measure(s).
To assess discriminant validity of the ASI-SR composite scores and external validity measures, an intercorrelation matrix between ASI-SR composite scores, and composite scores and external measures will be computed.
For evaluating factor structure principal component analyses (PCA) will be used.
Relevance for the field Opioid therapy for chronic non-cancer pain has emerged as a problematic treatment and the evidence is scarce for its effectiveness . However, there are some individuals that seem to benefit from opioid therapy and most guidelines propose an individual approach to management, beginning with a comprehensive patient evaluation, focusing on factors that may indicate potential substance use disorder. When opioids are used, clinicians should closely monitor patients for loss of response, adverse effects or aberrant behavior, and assess treatment outcome . There is a need for a multi-dimensional instrument that can assess problems related to increased risk for developing problematic opioid use, i.e. opioid use disorder, psychiatric co-morbidity and social problems. The ASI-SR could be an effective way of screening for current problems in different life domains and to monitor and evaluate ongoing treatment and identify problems if they would arise. Additional measures include urine or saliva drug testing, prescription practice, opioid treatment agreements, and universal precautions in conjunction with opioid therapy.
Ethical considerations The study will be sent to the Regional Ethical Review Board in Uppsala. Participants will be anonymous and all data will be coded before processed.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Chronic pain | – | Diagnostic Test: ASI-SRPatients with chronic non-cancer pain referred to secondary and tertiary care |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- In this days there are approx. 100 patients treated in the substitution program, 1300 patients receiving referral to the pain clinic in Uppsala Pain Center.
Key inclusion criteria (2 listed)
- Chronic non-cancer related pain
- ongoing treatment in the clinic
Key exclusion criteria (3 listed)
- severe cognitive impairment
- illiterate in Swedish
- inability to give informed consent.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ASI-SRPsychometric properties of ASI-SR | Diagnostic test | Chronic pain |
Primary outcome
Addiction Severity Index - Short version
Time frame: Baseline
The main objective with this study is to test the psychometric properties of the ASI-SR in a population of CNCP patients.Consistency of CS between the interview and the self-report will be evaluated on the individual basis by interclass correlation analysis (ICC) and at group level with paired t-test or Wilcoxon signed rank test if data is not normally distributed. ICC coefficient is considered to be poor if it is less than 0.40, fair between 0.40-0.59 , good between 0.60-0.70 and excellent between 0.75-1.00.
8 secondary outcomes
Patient Global Impression of Change
Time frame: Baseline
Addiction Severity Index -Short version
Time frame: 4-7 days later
Generalised Anxiety Disorder 7
Time frame: baseline
Research and Development 36-Item Health Survey RAND-36
Time frame: Baseline
Pain Disability Index
Time frame: Baseline
Alcohol Use Disorder Identification Test
Time frame: Baseline
Drug Use Disorder Identification Test
Time frame: Baseline
Patient Health Questionnaire PHQ9
Time frame: Baseline
Results and safety
The study was stopped early (reason given: Recruitment failure). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 May 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pernilla Åsenlöf, Profesor principal investigator
Uppsala University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Chronic Pain and Opioid-use Disorder, run by Uppsala University at 1 site in Sweden.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 11 May 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: Recruitment failure). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Addiction Severity Index - Short version (time frame: Baseline). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 May 2023.