Skip to content

Efficacy of Positive Mental Health Program for Adults - Study Protocol

Efficacy of Positive Mental Health Program for Adults

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04600401
Enrollment
60
Registered
2020-10-23
Start date
2020-05-15
Completion date
2021-12-31
Last updated
2020-10-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Health

Keywords

mental health, program, randomized controlled trial, nursing, health promotion, adult

Brief summary

The aim of this study is to evaluate the efficacy of a positive mental health program for adults, designated Mentis Plus+, in community. Our hypotheses are: 1. compared with the wait-list control group, the persons who join the experimental group and participate in the Mentis Plus+, will have more positive mental health on the end of the program; 2. in the Mentis Plus+ participants, positive mental health will be increased at the end of the program and at follow-up (three- six months later) and their psychological vulnerability will reduce.

Interventions

OTHERMentis Plus+ (Experimental Group)

Each factor can be considered a module, so it is a modular program. So, each module has 3 sessions to be carried out in full. It is a systematic program, so the order of the sessions is regulated by the letters A, B and C for each module. The modules to be worked on correspond to the low-level or languising factors identified after the application of the positive mental health questionnaire (PMHQ). After the application of the PMHQ, people are grouped with the same module to work.

Sponsors

Administração Regional de Saúde do Norte, Portugal
CollaboratorOTHER
Carme Ferré Grau
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Masking description

the researcher, who will collect the outcome assessments and assume data entry and analysis, will stay blinded to treatment allocations.

Intervention model description

Participants will be randomly allocated to either the Mentis Plus+ program (experimental group) or the control group (stand-by group).

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* to be a participant aged ≥ 18; * participant without a diagnosis of psychiatric pathology; * agree to participate in the program by signing informed consent; * participant with the low-level or languising in at least one factor of the positive mental health questionnaire

Exclusion criteria

* non-Portuguese speakers

Design outcomes

Primary

MeasureTime frameDescription
Psychological Vulnerability Scale (PVS) - moment 3PVS will be reapplied for follow-up of the evaluation, after completion of the study, on average 3 months, in both groupsThe PVS is a six-item scale. Each item is measured in a scale Frequency Likert five points (1-5), where a higher number corresponds to greater frequency (does not describe me at all = 1 to describes me very well = 5). Possible total scores range from 6 to 30, with higher scores indicating greater psychological vulnerability. greater psychological vulnerability.
Positive Mental Health Questionnaire (PMHQ) - moment 3The PMHQ will be reapplied for follow-up of the evaluation, after completion of the study, on average 3 months, in both groupsThe PMHQ consists of 39 items. In the PMHQ, values between 39 (minimum value) and 156 (maximum value) can be obtained, and higher the value obtained, lower the positive Mental Health level is. Therefore, we can categorize different levels of Positive Mental Health: High level or Flourishing (Results between 39-78), Intermediate level (Results between 79-117) and Low level or Languising (Results between 118-156).
Psychological Vulnerability Scale (PVS) - moment 1PVS will be applied in the baseline of the Mentis Plus+ Program, to both groupsThe PVS is a six-item scale. Each item is measured in a scale Frequency Likert five points (1-5), where a higher number corresponds to greater frequency (does not describe me at all = 1 to describes me very well = 5). Possible total scores range from 6 to 30, with higher scores indicating greater psychological vulnerability. greater psychological vulnerability.
Psychological Vulnerability Scale (PVS) - moment 2PVS will be applied up to 18 weeks of the Mentis Plus + Program,to both groupsThe PVS is a six-item scale. Each item is measured in a scale Frequency Likert five points (1-5), where a higher number corresponds to greater frequency (does not describe me at all = 1 to describes me very well = 5). Possible total scores range from 6 to 30, with higher scores indicating greater psychological vulnerability. greater psychological vulnerability.
Positive Mental Health Questionnaire (PMHQ) - moment 1PMHQ will be applied in the baseline of the Mentis Plus+ Program, to both groupsThe PMHQ consists of 39 items. In the PMHQ, values between 39 (minimum value) and 156 (maximum value) can be obtained, and higher the value obtained, lower the positive Mental Health level is. Therefore, we can categorize different levels of Positive Mental Health: High level or Flourishing (Results between 39-78), Intermediate level (Results between 79-117) and Low level or Languising (Results between 118-156).
Positive Mental Health Questionnaire (PMHQ) - moment 2PMHQ will be applied up to 18 weeks of the Mentis Plus + Program,to both groupsThe PMHQ consists of 39 items. In the PMHQ, values between 39 (minimum value) and 156 (maximum value) can be obtained, and higher the value obtained, lower the positive Mental Health level is. Therefore, we can categorize different levels of Positive Mental Health: High level or Flourishing (Results between 39-78), Intermediate level (Results between 79-117) and Low level or Languising (Results between 118-156).

Secondary

MeasureTime frameDescription
Sociodemografic and clinical data - moment 2Sociodemografic and clinical data will be applied up to 18 weeks of the Mentis Plus + Program,to both groupsGender, age, marital status, educational level, professional bond, displacement of usual residence, years of professional practice, hours of work per week, history of mental illness, health behaviors in the last month, consumption of psychoactive substances
Sociodemografic and clinical data - moment 3Sociodemografic and clinical data will be reapplied for follow-up of the evaluation, after completion of the study, on average 3 months, in both groupsGender, age, marital status, educational level, professional bond, displacement of usual residence, years of professional practice, hours of work per week, history of mental illness, health behaviors in the last month, consumption of psychoactive substances
Sociodemografic and clinical data - moment 1Sociodemografic and clinical data will be applied in the baseline of the Mentis Plus+ Program, to both groupsGender, age, marital status, educational level, professional bond, displacement of usual residence, years of professional practice, hours of work per week, history of mental illness, health behaviors in the last month, consumption of psychoactive substances

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026