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Enrolling by Invitation

NCT Number: NCT06822673

Impact of MBI on Biopsychosocial Factors and QOL in Children With Primary Headaches

* The Randomized Controlled Trial aims to evaluate the effectiveness of a Mindfulness-Based Intervention (MBI) in improving the quality of life and reducing psychological distress in children with primary headaches. This study focuses on children aged 8 to 12 years who experience primary headaches and aims to investigate the biopsychosocial factors influencing their well-being. * The primary objectives of this study are: * To assess the levels of mindfulness, emotional regulation, childhood traumatic experiences, psychological distress, and quality of life in children with and without primary headaches. * To identify the key biopsychosocial factors that impact the quality of life in children experiencing primary headaches. * To evaluate the effectiveness of mindfulness-based interventions in reducing psychological distress and enhancing the quality of life post-intervention. * To compare the differences between the intervention and control groups regarding their biopsychosocial well-being before and after the intervention. * To determine the long-term impact of the mindfulness-based intervention on psychological distress, quality of life, and headache frequency at a three-month follow-up. * Participants in the study will be screened from an initial survey, based on those experiencing headaches and randomly assigned to intervention and control groups. The intervention group will undergo a structured mindfulness-based program, while the control group will receive standard care. Data will be collected at baseline, post-intervention, and during follow-up assessments to measure the intervention's impact. * This study is significant as it aims to address the gaps in current research regarding pediatric primary headaches and their effect on psychological and social well-being. The findings may provide valuable insights for healthcare professionals to develop effective, non-pharmacological interventions to improve the quality of life of children suffering from primary headaches in Pakistan.

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Key information

Conditions

Primary Headache Anxiety Disorders Behavior Behavioral Symptoms Childhood Trauma Depression Emotion Regulation Emotional Regulation Health-Related Quality-of-Life Mental Disorders Mindfulness Psychological Distress Sedentary Behavior Sedentary Behaviors Self-Control Social Behavior

Age range

8 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fatima Jinnah Women University

Rawalpindi, 46000, Pakistan

About this study

Phases of the Study:

-Phase 1: Screening & Pre-Intervention Assessment Screening of children (ages 8-12) for primary headaches using standardized diagnostic criteria.

Assessment of biopsychosocial variables through validated psychological scales.

-Phase 2: Randomization & Intervention Random allocation of children into the intervention group, n=30 (receiving Mindfulness-Based Intervention) and control group, n=30 (receiving no intervention).

The intervention group would undergo an 8-week Mindfulness-Based Program, including techniques such as breathing exercises, guided imagery, body scanning, and mindful awareness practices.

-Phase 3: Post-Intervention Assessment Re-evaluation of all variables including psychological distress, mindfulness, and quality of life using the same assessment instruments.

Comparison of pre- and post-intervention outcomes.

-Phase 4: Follow-Up (3 Months Post-Intervention) Long-term impact assessment to determine sustained benefits of the intervention.

Ethical Considerations:

  • Informed Consent: Parents/guardians will provide written consent before participation.
  • Child Assent: Verbal and/or written assent will be obtained from children.
  • Confidentiality: All data will be anonymized and securely stored.
  • Right to Withdraw: Participants can leave the study at any point without any consequences.
  • Free Psychological Support: Children in the intervention group will receive completely free mindfulness-based therapy sessions, and participation in these sessions is voluntary.
  • After the study is completed, as an ethical and moral commitment, MBI therapy sessions would be offered to all those children also (who are willing) who were experiencing headaches but did not receive the intervention initially.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged between 8 to 12 years
  • From an initial survey, those who experience headaches would be screened
  • Children who are able to read and understand the English language, as the assessment instruments are in English, will be included.
  • Both the children and their parents must consent to the child's participation in the study.

Exclusion criteria

  • Children who are not students will be excluded from the study.
  • Children with any diagnosed genetic disease or disorder, chronic disease, or disability will be excluded.
  • Children with a current or past psychiatric disorder, especially those who have received treatment or medication for such conditions in the past year, will be excluded.
  • Children who have been on any long-term medication for any disease or disorder will be excluded, as this may influence the results of the study.

Treatment and study plan

Mindfulness Based Intervention

Behavioral

The Mindfulness-Based Intervention will include techniques derived from the Mindfulness Matters Program protocol (for Children and Adolescents, 2019). It will consist of both formal and informal practices, which participants will engage in during sessions and at home. These practices will encompass body scan meditation, mindful eating, mindful sitting, walking exercises, attention-focusing activities, and more. The intervention will be delivered over eight weekly sessions, following a skill-building, educational approach.

Primary outcomes

  1. Health-Related Quality-of-Life

    Time frame: 10-12 weeks

    • Health-Related Quality of life refers to an individual's overall physical, social and emotional well-being related to health.
    • Measurement Tool: Pediatric Quality of Life Inventory (PedsQL)
    • Unit of Measure: Total score on PedsQL, with higher scores indicating better quality of life.
    • Detail: The PedsQL consists of multiple items assessing the impact of health conditions on a child's daily functioning. The scale evaluates the overall Health-Related Quality of life by aggregating responses across all items and domains. The total score is computed as the mean of all responded items.

  2. Pediatric Headaches

    Time frame: 10-12 weeks

    • This outcome measure assesses the severity of headaches experienced by children.
    • Measurement Tool: Headache Screening Questionnaire (HSQ)
    • Unit of Measure: Total score, with higher values indicating greater headache severity.
    • Description: The HSQ consists of questions addressing headache related symptoms. This outcome would measure the changes in headache characteristics in response to MBI.

  3. Mindfulness

    Time frame: 10-12 weeks

    • Mindfulness refers to the practice of present moment awareness.
    • Measurement Tool: Child and Adolescent Mindfulness Measure (CAMM)
    • Unit of Measure: Total CAMM score, with higher scores indicating greater mindfulness.
    • Detail: Mindfulness will be evaluated to determine whether MBI changes children's ability to focus on the present moment.

Secondary outcomes

  1. Psychological Distress

    Time frame: 10-12 weeks

    • Psychological distress refers to the overall level of emotional discomfort or suffering experienced by an individual. It encompasses symptoms like anxiety, depression, and stress.
    • Measurement Tool: Depression Anxiety Stress Scales-Youth version (DASS-Y)
    • Unit of Measure: Total and subscale scores for depression, anxiety, and stress, with higher scores indicating greater distress.
    • Detail: The scale consists of 21 items, with seven items allocated to each of the three subscales: depression, anxiety, and stress. The overall aggregate score is then calculated to assess the individual's overall level of psychological distress.

    Psychological distress will be evaluated to determine the effectiveness of MBI related to emotional distress among children with primary headaches.

  2. Emotion Regulation

    Time frame: 10-12 weeks

    • Emotion regulation refers to the ability to handle emotions effectively. This measure is crucial in assessing how children regulate emotions, particularly in relation to stressful or painful experiences like headaches.
    • Measurement Tool: Emotion Regulation Questionnaire for Children and Adolescents (ERQ-CA)
    • Unit of Measure: Total score, with higher scores indicating better emotion regulation abilities.
    • Detail: This measure assesses children's ability to manage emotions effectively.

  3. Childhood Traumatic Experiences

    Time frame: 10-12 weeks

    • Childhood trauma includes adverse experiences such as abuse, neglect and other traumatic events.
    • Measurement Tool: Childhood Trauma Questionnaire-Short Form (CTQ-SF)
    • Unit of Measure: Total scores with higher scores indicating greater trauma exposure.
    • Detail: The scale assesses the cumulative impact of childhood traumatic experiences. The total score is used to evaluate the relationship between trauma exposure and primary headaches in children.

  4. Sedentary Behaviors

    Time frame: 10-12 weeks

    • Sedentary behaviors involve prolonged inactivity with minimal physical movement.
    • Measurement Tool: International Physical Activity Questionnaire (IPAQ) Short Form
    • Unit of Measure: Average hours per day spent in sedentary activities.
    • Description: The study will assess the effect of MBI on sedentary behaviors.

Sponsors and collaborators

Lead sponsor

Fatima Jinnah Women University

Other

Registry information

Official study title

Impact of Mindfulness-Based Intervention on Biopsychosocial Factors Associated With Quality of Life in Children With Primary Headaches: A Randomized Controlled Trial

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 12, 2025
Registry last updated
Feb 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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