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Persistent Physical Symptoms (PPS)NCT07912515

My Symptoms Young - a New Internet-based Programme for Young People With Persistent Physical Symptoms in Primary Care: Exploration of Effect and Health Literacy Characteristics Among Users

A study testing My Symptoms Young - an internet-based self-help programme for young people with persistent physical symptoms in people with Persistent Physical Symptoms (PPS) and Bodily Distress Syndrome, run by Aarhus University Hospital at 1 site in Denmark.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The research programme is an ambitious effort aiming to improve overall functioning and quality of life for young people with bodily distress. Bodily distress is a condition characterized by persistent physical symptoms (PPS), such as headache, nausea or abdominal pain, not explained by a well-defined disease. Read more about this study

Who is it for?
Ages 15 to 25 years
What is being tested?
My Symptoms Young - an internet-based self-help programme for young people with persistent physical symptoms
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
62 participants
Where
1 siteDenmark
Study dates
28 Nov 2025to 31 Dec 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

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 15 to 25 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Age: 15-25 years
  • Persistent or recurrent physical symptoms (PPS) ≥ 3 months
  • Average symptom intensity and interference of ≥ 3 on the NRS scale (0-10)
  • PPS affecting daily activities (e.g. school attendance, social activities, hobbies)
  • Symptoms are not explained by existing physical disease
  • Reads, speaks, and understands Danish

Who cannot join

  • Severe psychiatric or social problems (e.g. acutely suicidal, psychotic)
  • Problematic use of alcohol or drugs
  • Insufficient digital skills

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Nina Maindal contact

0045 61379813

ninmai@rm.dk

Charlotte Ulrikka Rask, Professor contact

charrask@rm.dk

Denmark1 site, 1 recruiting
  • Aarhus University Hospital

    Aarhus, 8200

    Nina Maindal, 0045 61379813, ninmai@rm.dk

    Charlotte Ulrikka Rask, Professor, charrask@rm.dk

    Recruiting

Other trials in Denmark

About this study

The research programme is an ambitious effort aiming to improve overall functioning and quality of life for young people with bodily distress. Bodily distress is a condition characterized by persistent physical symptoms (PPS), such as headache, nausea or abdominal pain, not explained by a well-defined disease. Over time, PPS can develop into a functional disorder, with detrimental impact on the young person's everyday life and opportunities. Thus, early intervention is crucial, but at present, access to specialized treatment of PPS to young people in primary care is very limited.

The investigators have developed the internet-based self-help programme My Symptoms Young as a new digital solution for early intervention of PPS. The intervention was developed using a high degree of user involvement (young people with PPS) and are now ready to be tested.

Read more

The goal of this clinical trial is to learn and preliminary test the possible effects of the internet-based self-help intervention program My Symptoms Young in young people aged 15-25 who experience PPS (physical symptoms presenting for >3 months). The main question the investigators aim to answer is:

  • What are the potential effects of My Symptoms Young In addition, the investigators aim to investigate if participation in the program can reduce overall symptom intensity and interference with daily activity in young people's lives. Finally, the investigators aim to examine if individual levels of health literacy (HL) and eHealth literacy (eHL) will modify the potential effects.
  • The primary outcomes will be symptom intensity and symptom interference with daily activities
  • The primary hypothesis will be: Symptom intensity and interference with daily activities will improve after the treatment with My Symptoms Young. The effect will be modified by levels of HL and aspects of eHL.

The investigators will include a total of 62 participants. The are no comparison group. Participants will be recruited from a health care professional in primary care (either general practitioner or practising pediatrician; from now on referred to as HCP). The HCP will determine whether referral to the My Symptoms Young programme is relevant. To guide this evaluation, the HCP will use pre-defined inclusion and exclusion criteria for participation. When a young person has been referred to the project group, a research assistent from the investigator group will contact the young person to provide more detailed information on the research project and the programme. If written consent is obtained, the young person will receive access to the programme. Throughout the intervention, the referring HCP is fully responsible for the health care of the young person. Referral and participation will be documented in the participants' primary care medical journal. If participants experience physical or psychological challenges during the project, they are advised to contact the referring HCP, i.e. the responsible healthcare provider.

The programme is accessed through a website, using either tablet, mobile or computer. It consists of seven modules, a closing module on relapse prevention, and a module targeting close relatives plus four tools: don't break the chain, goal setting staircase, symptom registration and notebook for reflections. The seven modules target symptom understanding, physical energy, resources and strains, thoughts, feelings, values, and self-care. Participants will gradually gain access to the modules. The programme encourages young persons to work with various exercises throughout the different modules but with freedom to choose what to work with. Besides text and exercises, the programme also includes explanatory animations, audio files on case stories, audio files on brief meditations and videos on physical exercises.

At first login (baseline), the participant will need to complete a set of questionnaires to access the programme. When completed the participant receives access to the programme. The researcher will follow up with participants by phone after one week if they have not logged into the programme and after three weeks if they have logged in but remained inactive. Participants can decide individually how long they wish to use the programme, but they are encouraged and recommended to engage actively at least twice a week for a minimum of 30 minutes. Participants will have access to the program for a total of 8 weeks. They will fill in questionnaires at three time points: Baseline (first login to the programme), End of Treatment (8 weeks after baseline) and 3 months after End of Treatment.

Read the detailed description

IDEA The research programme is an ambitious and dedicated effort aiming at the improvement of functioning and quality of life for young people with bodily distress. Bodily distress is a condition characterised by persistent physical symptoms (PPS) not explained by well-defined diseases. Over time, PPS can develop into a functional somatic disorder, with detrimental impact on the young person's everyday life and opportunities. Thus, early intervention is crucial, but at present, access to specialized treatment of PPS to young people in primary care is very limited.

The investigators have developed the internet-based self-help programme My Symptoms Young as a new digital solution for early intervention of bodily distress. The investigators have applied a high degree of user involvement (young people with PPS) in the development process and are now ready to test the possible impact of the resulting solution.

The present project will 1) test the impact of My Symptoms Young on young people (age 15-25 years) with PPS in primary care and 2) explore the influence of participants' health literacy (HL) and aspects of eHealth literacy (eHL) on their engagement with the programme and whether the level of HL and eHL modifies the impact. The latter might inform improvements regarding provision of adequate support for users with HL and eHL challenges.

BACKGROUND AND RATIONALE The decrease in mental well-being and the increase in distress among young people have become a critical public health concern. Young people with PPS such as pain and fatigue, which cannot be attributed to a specific well-defined disease, are common across various health care settings. Such symptoms are often an indicator of low mental well-being with different expressions of bodily distress, i.e. various physical responses to prolonged stress in susceptible individuals. PPS may cause school absence, high health-care costs, high medication use and low educational attainment. Additionally, PPS increases the risk of mental illnesses such as anxiety and depression. Furthermore, without intervention PPS may develop into severe functional somatic disorders (also classified as somatoform disorders in ICD-10/bodily distress disorder in ICD-11 or somatic symptom disorder in DSM-5), which often require resource-intensive specialized treatment in secondary care, including psychiatric settings.

Internet-based delivery methods allow for early provision of treatments otherwise only available in specialized care. The internet is prominent in young people's daily life and online resources e.g. mindfulness apps are publicly available but rarely target young people. Therefore, to address the treatment needs of youths (aged 15-25) with PPS in primary care, the investigators recently developed My Symptoms Young, a responsive application accessible via a web browser. Through user involvement, this internet-based intervention was redesigned from the existing My Symptoms programme for adults to meet the needs of young people. The content is mainly inspired by cognitive behavioral therapy and contains seven modules on symptom understanding, physical energy, resources and strains, values, thoughts, feelings, self-care, and in addition a closing module on relapse prevention. Furthermore, a module targeting close relatives is available to provide information and guide relatives on how to support participants to actively engage with the programme. Adherence is motivated by text message prompts 1-2 times a week. After a thorough usability evaluation My Symptoms Young is ready for the first clinical testing. However, the usability testing also revealed that some users can be challenged by understanding some of the provided information and exercises.

Health literacy (HL) may be an important precondition for young people's ability to engage with a treatment such as My Symptoms Young. Personal HL refers to individuals' ability to find, understand, and use information and services to inform health-related decisions and actions for themselves and others. Low HL has been linked to maladaptive health behavior and adverse illness perceptions in adults. In internet-based interventions active engagement depends not only on the abilities of the individual but also on the interaction between user and system as encompassed by the concept of eHealth Literacy (eHL). Thus, both HL and eHL characteristics in end users may be important to consider when testing and implementing a new eHealth intervention.

RESEARH AIMS, OVERALL STUDY DESIGN, AND METHODS Aim: To primarily test the possible effects of My Symptoms Young in young people with PPS.

Hypothesis: Symptom intensity and interference with daily activities will improve after the treatment with My Symptoms Young. The effect will be modified by levels of HL and aspects of eHL.

Study design: Open pilot study. Design and reporting will be in accordance with existing recommendations for non-randomized pilot studies.

Methods: 62 participants will receive questionnaires at three time points: Baseline (first login to the programme), End of Treatment (8 weeks after baseline) and 3 months after End of Treatment.

Primary outcomes will be symptom intensity and symptom interference with daily activities as measured by a numeric rating scale (NRS) ranging from 0 to 10. Secondary outcomes will reflect physical symptom burden, psychobehavioural features, health-related quality of life and satisfaction with the programme. HL and eHL measures at baseline will be applied as potential moderators of effect. Covariates will be participant sociodemographics, obtained at baseline, including data on age, gender, education, occupation/sick leave and self-reported chronic disease.

STUDY SETTING AND RECRUITMENT PROCEDURE The study is conducted in close collaboration with healthcare professionals (HCP) in primary care who are mostly likely to be in contact with young people with PPS in the early stage, namely general practitioners (GPs) and practicing pediatricians.

All recruiting HCPs will receive a guide outlining the information they must provide to participants during the recruitment process. Throughout the intervention, the referring HCP is fully responsible for the health care of the young person. Referral and participation will be documented in the participants' primary care medical journal. If participants experience physical or psychological challenges during the project, they are advised to contact the referring HCP, i.e. the responsible healthcare provider. This is also emphasized in the participant information.

RECRUITMENT PROCEDURE The recruitment procedure for the open pilot study can be divided in the following steps

  1. Young people with PPS will be recruited by a HCP in primary care. The HCP will determine whether referral to the My Symptoms Young programme is relevant.
  2. If the eligible participant is interested to learn more about the research project, the HCP will, with their approval, provide their Danish Personal Identification Number (CPR number) and contact information (phone/email) to the investigator group.
  3. When the investigators receives information on the eligible participant, written information material will be sent to the eligible participant through a secure system (eBoks).
  4. A research assistent from the investigator group will contact (via phone) the eligible participant, to schedule a video consultation.
  5. During the video consultation, a research assistant from the investigator group will provide verbal information about the project. The eligible participant will receive a presentation of the programme and guidance on how to log in and will also have the opportunity to ask questions. Finally study eligibility will be re-assessed and confirmed by the researcher.
  6. After ensuring that sufficient verbal information has been provided, informed consent will be obtained. Written consent forms will be collected electronically via a unique link to the consent form hosted on the secure web-based data collection platform, REDCap.
  7. Once written consent is obtained, a research assistent from the investigator group will provide the participant with a login code (via e-Boks) to access the programme at www.mine-symptomer.dk. The research assistent will encourage the participant to log in to the programme within a few days.
  8. The research assistent will notify the referring HCP about participation (via phone or email).
  9. The HCP will then document the referral in the participant's medical journal.

When the participant has signed the consent form, they login to a web portal via the website and access the internet-based programme. The programme is secured by two-factor authentication. The participant login with an unique national electronic identifier (MitID) and a code subsequently provided by the app MitID. Finally, they will need to provide the code provided by the research assistent. At first login, the participant will need to complete a set of questionnaires before accessing the programme. When completed the participant receives access to the programme. The research assistent will follow up with participants by phone after one week if they have not logged into the programme and after three weeks if they have logged in but remained inactive. Participants can decide individually how long they wish to use the programme, but they are encouraged and recommended to engage actively at least twice a week for a minimum of 30 minutes.

The research assistent will contact all participants for an end-of-treatment interview (8 weeks after baseline). The interview will be conducted via telephone and will not be recorded. The aim will be to gather their overall feedback/comments on the programme, and to recommend that the participant engage in a follow-up consultation with their referring HCP. Additionally, participants will be reminded to complete the End of Treatment questionnaire (8 weeks after baseline), and the 3-months follow up questionnaire, which will be delivered via e-Boks.

DATA COLLECTION The study will make use of self-reported questionnaire data from the participating young person and data retrieved from the My Symptoms Young-programme. Participant questionnaires will be administered at baseline (first login to the programme), Endof Treatment (8 weeks after baseline) and 3 months follow-up after End of Treatment. Participant data from the internet-based programme will also be retrieved at End of Treatment (8 weeks after baseline).

Self-report questionnaires

Time points of questionnaire distribution:

Time point 1: Baseline (first login to the programme) Time point 2: End of Treatment (corresponding to 8 weeks after first login) Time point 3: 3-month follow-up after End of Treatment.

Data retrieved from the internet-based programme

The investigators will keep track of young person's eventually accepting and logging into the programme and describe their use of the programme. Their work is logged with regard to:

  • Number of logins
  • Number of days with login
  • Number of modules visited
  • Number of visits on every single "page" in the programme
  • Number of exercises created using the provided tools.
  • Total time spent in the programme
  • Time spent per programme module.

INTERVENTION The development of the intervention My Symptoms Young and the subsequent evaluation follows the principles for complex interventions as suggested by the Medical Research Council (MRC-guideline) in 2021.

Development of the My Symptoms Young The current project has been preceded by an iterative development of the first prototype of the intervention supported by the Quality Improvement Committee for General Practice of the Region of Southern Denmark (Kvalitets- og Efteruddannelsesudvalget i Region Syddanmark), J.no.: 20/37140 and the joint regional fund under Danish Regions (Den fælles regionale pulje under Danske Regioner), J. no. EMN-2019-00852 1310643. My Symptoms Young is based on the existing My Symptoms programme for adults and is through user involvement and usability testing redesigned to meet the specific needs of young people.

The process involved a review of evidence on existing self-help interventions for young people with PPS, identification of specific user needs through a qualitative interview study with 11 young people with PPS and usability testing in the further development and refinement of the content of the self-help intervention. Specific modifications have included reduction and simplification of text, adaption of case stories to content relevant for the age group, more focus on suggesting involvement of the family and other close relatives in the programme content and exercises to get support and encouragement.

Content of 'My Symptoms Young' My Symptoms Young is an internet-based self-help programme developed specifically to young persons with moderate PPS seen in primary care. It is designed so the HCP can refer the young person to the programme, when the HCP finds it relevant according to the guiding in- and exclusion criteria.

The young person will get access to an advanced internet-based programme consisting of seven modules, a closing module on relapse prevention, and a module targeting close relatives plus four tools: don't break the chain, goal setting staircase, symptom registration and notebook for reflections. The seven modules target symptom understanding, physical energy, resources and strains, thoughts, feelings, values, and self-care. Participants will gradually gain access to the modules.

The module for close relatives is designed to inform them about the program's content and what participants will experience. It also provides advice and guidance for relatives to support participants in successfully completing the programme. The closing module targets questions for reflection on personal outcome, statistics on work in the programme, results on the Bodily Distress Syndrome (BDS) checklist and relapse prevention. The programme encourages young persons to work with various exercises throughout the different modules but with freedom to choose what to work with. Besides text and exercises, the programme also includes explanatory animations, audio files on case stories, audio files on brief meditations and videos on physical exercises.

ANALYSIS AND STATSTICS Descriptive analyses of participant characteristics, primary and secondary outcomes, and HL and aspects of eHL will be performed at baseline. Linear regression models will be used to analyze the potential changes in outcomes from pre-treatment to post-treatment and three months follow-up. Levels of HL and eHL, respectively, will be added as continuous scores in separate analyses to test their impact on outcomes. If feasible the analyses will be adjusted for sociodemographic characteristics and presence of chronic disease.

Sample size calculation: Sample size is based on a power analysis performed for the adult programme My Symptoms using the same primary outcome, i.e. symptom intensity: detecting a true change in the primary outcome with a probability of 80%, alpha level set at 0.05 and the correlation between measurements in the same individual at baseline and post-treatment assumed to be 0.7, a minimum sample size of 62 would be required, assuming a mean difference of 0.52 and a standard deviation of 0.14 (based on effects reported on eHealth treatment for adults with chronic pain).

ETHICS AND DATA PROTECTION The study will be conducted in accordance with the Declaration of Helsinki and has received approval from the Research Ethics Committee of the Central Denmark Region (reference no. 1-10-72-52-25).

The study has also been registered in the Central Denmark Region's internal research project register (reference no. 1-16-02-266-25) and in Aarhus University's record of processing activities in accordance with Article 30 of the General Data Protection Regulation (GDPR) (reference no. 2022-0367531, registration no. 3892).

All personal data will be processed in compliance with the GDPR and the Danish Data Protection Act, including Section 10, which regulates the processing of personal data for scientific research purposes. Participants will receive written information about the study, including how their personal data will be processed.

EXPECTED OUTCOMES Overall, the intervention is expected to improve the health of young persons with bodily distress in the form of PPS, their functioning and quality of life at an early stage, i.e. before the symptoms become chronic. As part of symptom assessment and management, the HCP will have to draw on physical examinations and potential biomedical investigations etc., but the current programme may both empower the young person and improve how the HCPs in primary care communicate with young people about PPS, hence have the potential to reduce the use of health care, improve symptom coping and illness perception.

The investigators expect the intervention to be able to reduce symptom intensity and interference with daily activities. Over time the investigators expect a reduce in health care use. Thus, part of the idea behind the programme is to move time-consuming information about symptoms from the consultation to the young person's home. Use of primary care may increase temporarily as seen in previous intervention studies, but use of secondary hospital-based health care is expected to decrease.

ADVERSE EVENTS There are no expected side effects or risks in participating in the study. Thus, there are no known harmful effects of internet-based self-help interventions to young people, neither short nor long-term. The disadvantage of participation is mainly the need to spend time with the programme and the scientific evaluation (questionnaires).

Being tested
My Symptoms Young - an internet-based self-help programme for young people with persistent physical symptoms
Keywords
Persistent physical symptoms, Young people, Internetbased interventions, Bodily distress, Health literacy, eHealth literacy, iCBT

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • My Symptoms Young - an internet-based self-help programme for young people with persistent physical symptomsOther

    My Symptoms Young is advanced internet-based self-help programme consisting of seven modules, a closing module on relapse prevention, and a module targeting close relatives plus four tools: don't break the chain, goal setting staircase, symptom registration and notebook for reflections. The seven modules target symptom understanding, physical energy, resources and strains, thoughts, feelings, values, and self-care. The program is accessed through a website using either a computer, tablet or mobile phone.

Study groups in NCT07912515
Study groupRoleWhat they receive
My Symptoms Young ParticipantsExperimentalParticipants aged 15-25 experiencing persistent physical symptoms (≥3 months), referred to the 8-week internet-based intervention My Symptoms Young.
Receives: Other: My Symptoms Young - an internet-based self-help programme for young people with persistent physical symptoms

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Symptom intensity and interference

    The primary outcomes will be symptom intensity and symptom interference with daily activities as measured by a numeric rating scale (NRS) ranging from 0 to 10. For symptom intensity, the young person rates the overall intensity of their bodily symptoms within the past 7 days where 0 represents 'no symptoms at all' and 10 'worst possible symptoms'. For symptom interference, the young person indicates their bodily symptoms' interference with daily activities within the past 7 days, 0 will represent 'Not at all' and 10 'Interfered completely'

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

Secondary outcomes (10)
  1. SF-36

    Two items from the SF-36 score will be used to measure overall global health. The first item is "In general, would you say your health is" and is rated on a Likert scale 1 (excellent), 2 (very good), 3 (good), 4 (fair) and 5 (poor). The second item is "Compared to one year ago, how would you rate your health in general now". The item is rated on a Likert scale ranging from 1 (much better now than one year ago), 2 (somewhat better now than one year ago), 3 (about the same), 4 (somewhat worse now than one year ago) and 5 (much worse now than one year ago)

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  2. The Bodily Distress Syndrome (BDS) Checklist

    The Bodily Distress Syndrome (BDS) Checklist will be administered as a measure of physical symptom burden. The BDS Checklist explores the presence of 25 symptoms representing four symptom clusters: cardiopulmonary, gastrointestinal, musculoskeletal, and general symptoms. The young person will be asked to rate on a 5-point Likert-type scale how much they have been bothered by each of the 25 listed symptoms within the past four weeks. Response categories are: 'not at all' (0), 'a bit' (1), 'somewhat' (2), 'quite a bit' (3) and 'a lot' (4). The sum score will be calculated by adding the single item scores from the 25 items (range 0-100) with higher scores representing higher symptom burden.

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  3. The Limitation Index (LI-index)

    Impact on physical functioning will be measured using the Limitation Index (LI-index). The questionnaire is a modified version of the Pain Interference Index (PII), which emphasizes symptoms beyond just pain. The PII was developed as a brief instrument to assess the impact of pain on behaviours and the extent to which long-standing pain interferes with essential aspects of daily life. The modified LI-index consist of six items that measures the extent to which physical symptoms have limited behaviour within the past four weeks. The items are rated on a Likert scale ranging from 0 ('not at all') to 6 ('very much').

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  4. Patient Global Impression of Change (PGIC)

    Self-rated global health change will be obtained using the Patient Global Impression of Change (PGIC) scale. The young person will be asked to rate current health condition on a five-point Likert scale ranging from much worse to much better health. For statistical analysis, the scale will be collapsed into three categories representing much improved, minimal or no change and much deteriorated health. Based on the NRS of symptom intensity, the proportion of young persons that has clinically significantly improved will be calculated. Clinically significant improvement will be defined as a decrease in symptom intensity of ≥2.0 points. Adverse events will be defined as a 50% worsening of symptoms as measured by the NRS for symptom intensity.

    Measured: End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  5. The Brief Illness Perception Questionnaire (B-IPQ)

    To measure illness perception, an adapted version of the Brief Illness Perception Questionnaire (B-IPQ) will be used. The original B-IPQ has 9 items; 5 items assess cognitive illness representations such as consequences, timeline, personal and treatment control, and identity. Two items assess emotional representations such as concerns and emotions and finally, illness comprehensibility and illness causes are assessed by one item respectively. Apart from illness causes, each item is scored on a scale ranging from 0-10. PPS is not an illness per se and young persons with PPS may not have a diagnosis. Therefore, the investigators have replaced the term 'illness' with 'symptoms'. Therefore, one item 'How much do you experience symptoms from your illness?' has been removed. A total score (range 0-70) will be calculated with lower scores indicating more positive illness perceptions.

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  6. The Behavior Related to Illness Questionnaire (BRIQ)

    Two subscales from the Behaviour Related to Illness Questionnaire (BRIQ) will be applied to measure behavioural responses to PPS within the past four weeks. The subscale "Limiting behaviour" comprises 6 items and the subscale "All or nothing behaviour" 7 items. All items are scored on a 5-point Likert-type scale representing the frequency of certain behaviours and ranging from 0 ('not at all') to 4 ('every day'). For each subscale, a sum score will be calculated with lower scores indicating a more adaptive symptom behaviour.

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  7. Pain Self-Efficacy Questionnaire (PSEQ)

    To measure participants' current confidence in performing activities in the context of PPS, an adapted version of the Pain Self-Efficacy Questionnaire (PSEQ) is used. To address young people with PPS, the term 'pain' has been replaced by 'symptoms'. The PSEQ comprises ten items that are scored on a 7-point Likert-type scale ranging from 0 ('not at all confident') to 6 ('completely confident'). A sum score (range 0-60) will be calculated.

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  8. Whiteley Index (WI-6-R)

    Illness worry is measured using the revised version of the six-item Whiteley Index (WI-6-R). The WI-6-R measures to which extent the respondent within the past four weeks has been bothered by fear of being ill and has attributed current bodily sensations to physical disease. The six items are rated on a Likert-type scale ranging from 0 ('not at all') to 4 ('very much'). A sum score (range 0-24) will be calculated with higher scores indicating higher illness worry.

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  9. Symptom Checklist (SCL-90)

    Impairment by anxiety and depression will be measured with subscales from the Danish version of the Hopkins Symptom Checklist (SCL-90), the SCL-ANX4 for anxiety and the SCL-DEP6 for depression. Each item in these subscales relates to the past four weeks and is rated on a five-point Likert scale of distress ranging from 'not at all' (0) to 'very much' (4). The total sum scores will be calculated for each subscale (range: anxiety 0-16, depression 0-24). Higher scores indicate higher impairment.

    Hopelessness will be measured by one item from the SCL-90: "During the last four weeks, how much were you bothered by feelings of hopelessness about the future?". Response categories are measured on a five-point Likert scale ranging from 'not at all' (0) to 'very much' (4).

    Measured: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment

  10. Use of health care services

    Twelve individual items will be used to assess participants' use of healthcare services and medication consumption over the past three months. Eight items refer to the number of consultations participants have had with various healthcare professionals, including general practitioners, social workers, manual therapists, occupational therapists, dietitians, alternative practitioners, psychologists, psychotherapists, or psychiatrists, and private specialist doctors. Participants can either indicate that they have had no consultations at all or specify the number of visits. Additionally, three items assess whether participants have visited an emergency department, had outpatient consultations, or been hospitalized. The response categories are the same as in the previous section. Finally, one item evaluates medication consumption. Participants will be asked whether they have taken painkillers, medication for anxiety or depression, diuretics, weight-loss medication, or protein supplements.

    Measured: Baseline (first login in programme), 3-months after End of Treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Nov 2026
  2. Study start28 Nov 2025
  3. Primary completion30 Sep 2027 (estimated)
  4. Study completion31 Dec 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
62 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07912515
Sponsor's protocol ID
1-16-02-266-25
Other IDs
3166-00018A, 158761, 03/20
Status last verified
Oct 2026
First submitted
26 Oct 2026
Last updated
3 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Christensen OR, Hedegaard L, Rask MT, Clemensen J, Frostholm L, Rosendal M. Designing and Developing an eHealth Program for Patients With Persistent Physical Symptoms: Usability Study. JMIR Hum Factors. 2023 Feb 8;10:e42572. doi: 10.2196/42572.

    PubMed 36753312
  • Vigerland S, Lenhard F, Bonnert M, Lalouni M, Hedman E, Ahlen J, Olen O, Serlachius E, Ljotsson B. Internet-delivered cognitive behavior therapy for children and adolescents: A systematic review and meta-analysis. Clin Psychol Rev. 2016 Dec;50:1-10. doi: 10.1016/j.cpr.2016.09.005. Epub 2016 Sep 20.

    PubMed 27668988
  • Rosendal M, Blankenstein AH, Morriss R, Fink P, Sharpe M, Burton C. Enhanced care by generalists for functional somatic symptoms and disorders in primary care. Cochrane Database Syst Rev. 2013 Oct 18;2013(10):CD008142. doi: 10.1002/14651858.CD008142.pub2.

    PubMed 24142886
  • Aaby A, Friis K, Christensen B, Rowlands G, Maindal HT. Health literacy is associated with health behaviour and self-reported health: A large population-based study in individuals with cardiovascular disease. Eur J Prev Cardiol. 2017 Nov;24(17):1880-1888. doi: 10.1177/2047487317729538. Epub 2017 Aug 31.

    PubMed 28854822
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Questions about this trial

What is this clinical trial studying?

A study testing My Symptoms Young - an internet-based self-help programme for young people with persistent physical symptoms in people with Persistent Physical Symptoms (PPS) and Bodily Distress Syndrome, run by Aarhus University Hospital at 1 site in Denmark.

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 6 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: looking for participants now, as of the sponsor's last update on 3 Nov 2026. 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 Denmark. 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?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Nina Maindal (0045 61379813, ninmai@rm.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Symptom intensity and interference (time frame: Baseline (first login in programme), End of Treatment (8 weeks after baseline), 3-months after End of Treatment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07912515, which also lists 11 linked publications.

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 3 Nov 2026.

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