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Completed

NCT Number: NCT05216445

Mindfulness for Stress and Well-being in University Students

In developing countries such as Pakistan, the challenges university students face are many-fold and there is a need for an intervention that helps build students' connection with themselves, utilizing their internal resources to deal with stresses. Mindfulness-based interventions have shown effectiveness with university students in high-income countries. The current study will be testing an adaptation for students of Pakistan of an intervention (Finding Peace in a Frantic World) which is based on principles from both Mindfulness-based cognitive therapy(MBCT) and Mindfulness-based stress reduction(MBSR). The purpose of this pilot trial is to assess the feasibility and acceptability (primary outcomes) of conducting a randomized controlled trial (RCT) of an adapted Mindfulness-based intervention with a wait-list control group for university students in Pakistan to reduce stress and enhance psychological well-being (N=50), which will inform the development of a future large-scale RCT. Keeping in view the COVID-19 lockdown and economic conditions in low-and-middle-income countries (LAMICs), an online program with a remote facilitator is deemed to be more cost-effective, approachable, practical, and de-stigmatizing for students.

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Key information

Conditions

Stress Well-Being

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National University of Science and Technology

Islamabad, Punjab Province, 44000, Pakistan

About this study

In LAMICs, including Pakistan young adults comprise more than half of the total population (60%) many of them enrolled in universities (12.7% of the total young adult population) emphasizes the need for psychological interventions in these educational institutes.

Considering the substantial lack of a systematic approach in the development, adaptation, and implementation of mindfulness-based interventions the investigators of this study employed the first two steps of Medical Research Council Guidelines (MRC) for the development of complex interventions. This current study represents the final phase of the project, where the feasibility and acceptability of the Adapted Mindfulness Training will be assessed through a Pilot RCT. The participants will be randomly assigned to either the Mindfulness Training group or the wait-list control group. The participants in the Mindfulness Training group will have online 8-week training, with weekly online group video-conference sessions with the facilitator. Both groups will be asked to complete questionnaires for outcome measures (mindfulness, well-being and stress), one week before the training starts and one week after the training ends. At the end of the training semi-structured interviews about the training will be conducted with participants (from the Mindfulness Training) who consent. The study will examine key methodological uncertainties (recruitment methods, recruitment rate, retention rate, randomization procedures), explore the acceptability of the adapted intervention and calculation of appropriate sample sizes and preliminary responses to the intervention in order to inform a future large-scale RCT. Acceptability here refers to the assessment of whether the university students find it appropriate and according to their needs and culture. To the investigator's knowledge, there haven't been any RCTs that studied the effectiveness of an online Mindfulness training translated in Urdu and adapted for university students in Pakistan to reduce stress and enhance well-being.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 18 years or older
  • enrolled in an undergraduate or postgraduate course in a university in Pakistan.

Exclusion criteria

  • suffering from any current diagnosed severe mental illnesses including severe depression, anxiety, hypomania, or psychotic illness
  • suffering from any severe medical illness.

The criteria will be self-reported by the students at the time of registration for the training.

Treatment and study plan

Mindfulness Training

Behavioral

The Mindfulness Training will be an 8-week course, with group-based online weekly sessions. The mindfulness training, translated and adapted in Urdu, includes 8 guided audio meditations and one introductory audio recording which gives the participants an overview and introduction of the forthcoming 8-week training (e.g what mindfulness is, some common terms used repeatedly). It also includes 8 chapters, corresponding to each week and a workbook to record home practice. The training will start with an online group session after which the participants will be emailed the 1st week's reading material (chapter 1), audio recordings (for that week), home practice (for that week). At the start of every week, the participants will be emailed the required material for that week. Online sessions will be conducted weekly. The participants will also be sent poems and/or quotations relating to the week's theme and based on the session proceedings.

Primary outcomes

  1. Feasibility- recruitment method

    Time frame: 3 months

    The number of participants recruited by each of the four methods used for recruiting. The four methods will be: social media and student groups, university platforms, referrals and recommendations and direct email to students.

    The barriers and facilitators in each method will evaluated by the recruiters.

  2. Feasibility-recruitment rate

    Time frame: 3 months

    Recruitment rate will be assessed through the number of participants who registered, number of participants screened through eligibility criteria, number of participants who start the training.

  3. Feasibility of videoconferencing

    Time frame: 3 months

    The assessment of barriers in technology including number of participants unable to attend sessions due to connectivity issues, number of participants dropped during sessions due to technical problems, number and type of problems, the number of participants seek extra time due to technical problems. The utility of zoom videoconferencing functions.

  4. Feasibility-flexible multiple weekly online sessions

    Time frame: 2 months

    The assessment of difficulties in conducting a multiple group format on both Saturday and Sunday for each weekly online session.

  5. Feasibility- eligibility criteria

    Time frame: 3 months

    Assessed through number of participants fulfilling the eligiblity criteria from the total number of students registered, number of ineligible participants and reasons for ineligibility.

  6. Videoconferencing - acceptability by students

    Time frame: 3 months

    The acceptability of videoconferencing by students will be assessed in terms of ease of use (1=not at all, 5= very much; post-intervention survey), interference of technical problems (1=not at all, 5= very much; post-intervention survey), advantages and disadvantages, overall satisfaction (1=poor, 5=excellent; post-intervention survey), suggestions for improvement (feedback interview)

  7. Acceptability - Attrition rates

    Time frame: 3 months

    The number of participants who complete the training and assessments, number of participants who withdraw and drop out, reasons for withdrawal and dropout.

  8. Acceptability -participant attendance in weekly online sessions

    Time frame: 2 months

    Average number of sessions attended by participants, reasons for missing sessions

  9. Acceptability-Home practice

    Time frame: 2 months

    Number of participants who submit weekly worksheets, average number of worksheets submitted by participants, the different tasks completed, time spent in home practice (post-training survey).

  10. Acceptability of mindfulness training by students- semi-structured interview

    Time frame: 3 months

    The interview will explore students' overall satisfaction with the adapted MBI, their perception of any possible facilitators and barriers in taking part in the adapted MBI, any system changes experienced (including familial and community relationships), any physical/ psychological adverse effects or benefits experienced during and after the adapted MBI, the students' view about the mindfulness exercises and daily tasks used in the adapted mindfulness-based intervention, the group format, the home practice, any suggestions for improvement.

  11. Feasibility of conducting the trial -randomization

    Time frame: 3 months

    The types and number of difficulties in randomization.

  12. Acceptability of randomization

    Time frame: 3 months

    The number of participants who consented for randomization, number of participants who refused, number of participants who changed their group, reasons for refusal and change of group.

  13. Feasibility of online data collection

    Time frame: 3 months

    The procedures of outcome measures data collection procedures, and online feedback interviews

  14. Feasibility- outcome measures

    Time frame: 3 months

    Feasibility of outcome measures will be assessed through the assessment completion rates by participants.

Secondary outcomes

  1. Psychological well-being Scale

    Time frame: baseline assessment before the delivery of intervention and after 8 weeks i.e the completion of intervention

    Psychological well-being Scale is used as a measure of psychological well-being with six categories; autonomy, environmental mastery, personal growth, positive relations with others, purpose in life and self-acceptance. It consists of 42 items rated on a Likert scale ranging from 1=strongly disagree to 4=strongly agree. Higher scores indicate higher levels of psychological wellbeing.

  2. Five Facet Mindfulness Questionnaire

    Time frame: baseline assessment before the delivery of intervention and after 8 weeks i.e the completion of intervention

    Five Facet Mindfulness Questionnaire is used as a measure of dispositional mindfulness. It consists of 39 items rated on a Likert scale ranging from 1=never or very rarely true to 4=very often or always true. Higher scores indicate increase in mindfulness.

  3. Clinical Outcomes Routine Evaluation-Outcome Measure

    Time frame: baseline assessment before the delivery of intervention and after 8 weeks i.e the completion of intervention

    Clinical Outcomes Routine Evaluation-Outcome Measure is used as a measure of psychological distress. It consists of 34 items rated on a Likert scale ranging from 1=not at all to 4=most of the time. Higher scores indicate higher levels of psychological distress.

Sponsors and collaborators

Lead sponsor

National University of Science and Technology, Pakistan

Other

Registry information

Official study title

An Adapted Mindfulness-based Intervention for Stress Reduction and Psychological Well-being of University Students in Pakistan: a Pilot Randomized Trial Protocol

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jan 31, 2022
Registry last updated
May 11, 2022

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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