Stress Clinical Trial
Official title:
An Adapted Mindfulness-based Intervention for Stress Reduction and Psychological Well-being of University Students in Pakistan: a Pilot Randomized Trial Protocol
| Verified date | May 2022 |
| Source | National University of Science and Technology, Pakistan |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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.
| Status | Completed |
| Enrollment | 157 |
| Est. completion date | April 30, 2022 |
| Est. primary completion date | April 30, 2022 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | 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. |
| Country | Name | City | State |
|---|---|---|---|
| Pakistan | National University of Science and Technology | Islamabad | Punjab |
| Lead Sponsor | Collaborator |
|---|---|
| National University of Science and Technology, Pakistan |
Pakistan,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Feasibility- recruitment method | 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. |
3 months | |
| Primary | Feasibility-recruitment rate | 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 months | |
| Primary | Feasibility of videoconferencing | 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. | 3 months | |
| Primary | Feasibility-flexible multiple weekly online sessions | The assessment of difficulties in conducting a multiple group format on both Saturday and Sunday for each weekly online session. | 2 months | |
| Primary | Feasibility- eligibility criteria | Assessed through number of participants fulfilling the eligiblity criteria from the total number of students registered, number of ineligible participants and reasons for ineligibility. | 3 months | |
| Primary | Videoconferencing - acceptability by students | 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) | 3 months | |
| Primary | Acceptability - Attrition rates | The number of participants who complete the training and assessments, number of participants who withdraw and drop out, reasons for withdrawal and dropout. | 3 months | |
| Primary | Acceptability -participant attendance in weekly online sessions | Average number of sessions attended by participants, reasons for missing sessions | 2 months | |
| Primary | Acceptability-Home practice | 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). | 2 months | |
| Primary | Acceptability of mindfulness training by students- semi-structured interview | 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. | 3 months | |
| Primary | Feasibility of conducting the trial -randomization | The types and number of difficulties in randomization. | 3 months | |
| Primary | Acceptability of randomization | 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. | 3 months | |
| Primary | Feasibility of online data collection | The procedures of outcome measures data collection procedures, and online feedback interviews | 3 months | |
| Primary | Feasibility- outcome measures | Feasibility of outcome measures will be assessed through the assessment completion rates by participants. | 3 months | |
| Secondary | Psychological well-being Scale | 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. | baseline assessment before the delivery of intervention and after 8 weeks i.e the completion of intervention | |
| Secondary | Five Facet Mindfulness Questionnaire | 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. | baseline assessment before the delivery of intervention and after 8 weeks i.e the completion of intervention | |
| Secondary | Clinical Outcomes Routine Evaluation-Outcome Measure | 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. | baseline assessment before the delivery of intervention and after 8 weeks i.e the completion of intervention |
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