Mindfulness-Based-Cognitive-Intervention for African Caribbean Men With Erectile Dysfunction

Sponsor
London Metropolitan University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05167955
Collaborator
(none)
40
1
2
9.8
4.1

Study Details

Study Description

Brief Summary

Title of research: A preliminary Randomised Controlled Study online Mindfulness-Based-Intervention for African-Caribbean men with Erectile Dysfunction

Research aim: How an online mindfulness intervention, based on a behavioral health taxonomy, might reduce symptoms of erectile dysfunction and increase sexual well-being among African-Caribbean men in the United Kingdom.

Research intention: If the Mindfulness-based intervention reduces symptoms of erectile dysfunction and increases sexual wellness, then we would repeat this study on a larger scale among Black, Asian, Minority, and Ethnic men via the National Health Service.

A brief overview of intervention: Erectile dysfunction is the inability to achieve or maintain an erection in up to 75 to 100% of sexual attempts, including masturbation and sexual intercourse. It is typically very costly to treat on the National Health Service, using the combination of medication (e.g. Viagra) and psychosexual therapy.

The use of mindfulness in healthcare for varied psychosocial difficulties is gaining popularity. A meta-analysis on mindfulness and sexual dysfunction among men and women. Whilst gender differences were the priority focus of the analysis, it also looked at how well-represented cultural and minority groups were within the existing clinical trials. The review identified no studies relating to Black, Asian, Minority and Ethnic men with erectile dysfunction and mindfulness.

Quantitatively, the research is structured so that participants will be randomized to either the experimental or control group (n=20 experimental; n=20 control waitlist). A 3-month follow-up will be taken to determine the sustainability of this intervention. Qualitatively, participants will be asked approx 10 open-ended questions forming part of 8 focus groups of 5, at the 3-month follow-up.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness based cognitive intervention based on the behavioural change techniques taxonomy
N/A

Detailed Description

The principal researcher developed the online mindfulness cognitive intervention. An understanding of the intervention along with educational sessions about erectile dysfunction will be carried out among the team. Part of this programme will involve the research assistants who will overview the implementation of the assessments and pre and post output measurements of the intervention. The mindfulness box will include an array of educational material and cognitive templates on erectile dysfunction and sexual behaviour education. The mindfulness specialist will deliver the intervention. In total, 15 domains have been included in the development of this intervention. Of these, 35 out of the 93 behavioral change techniques taxonomy were identified.

The main targets here are to engage those with mindfulness exercises whilst improving wellbeing and minimizing erectile dysfunction. This will aim to show salience of consequences where feedback will emphasize the positive outcomes of performing the mindfulness-based cognitive intervention. The main exercises include mindfulness, breathing exercises, relaxation techniques, being mindful of the senses and the body, and understanding of the self. Each of the 4 sessions will be between 2-3 hours long where at-home exercises will be encouraged. Additionally, four one-hour online group chats will be available until wk 4. Feedback and support along with discussing the educational components, training, modelling and enablement will be addressed throughout. As the content of the randomized controlled study online mindfulness-based cognitive intervention is, the specific intervention targets described in table 1 have included cognitive, emotional, or behavioral factors or a combination of these.

Table 1

Techniques within this Intervention target Behaviour change techniques taxonomy Randomised controlled study

Cognitive

Psychoeducation Understanding erectile dysfunction 4.2, 5.1, 5.3, 5.5, 5.6, 9.2 The hot cross bun

Sexual self-efficacy Enjoyable sex 1.2,1.4, 1.9, 2.3, 11.2, 15.3,16.2

Cognitive reframe/self talk Challenging thoughts associated 4.3, 11.2, 13.2, 15.4 with sexual performance

Behavioural

Reward and reinforcement Encourage new behaviour coupled 1.2, 1.4, 4.1, 8.1, 8.2 with positive feedback 10.7, 10.10, 11.2, 14.4

Self-care Behaviours which promote physical 10.7, 10.10 mental and emotional well-being

Self-monitoring Monitor behaviour towards goals 1.1, 1.2, 1.3, 1.4, 1.9, 2.2, 2.3, 2.7

Mindfulness-based cognitive intervention

Understanding emotions Recognising and developing emotions 1.2, 3.1, 5.6, 8.1, 11.2 and coping strategies 12.4

Goal setting/smart goals Specific, Measurable, Achievable, 1.1, 1.2, 1.3, 1.4, 1.9, 2.2,2.3,2.7 Realistic and anchored within a Time Frame.

Self-directed meditation Creating better awareness of 1.9, 4.1, 6.1,8.1, 11.2,15.2 body, mind and breathing

Body scan Bringing attention and awareness 4.1, 6.1, 8.1, 11.2, 15.2 to different areas of the body. Top to toe.

Mindfulness practices Being aware of the present moment 4.1, 6.1,8.1, 11.2, 12.6 15.2, 16.2

Mindfulness stretching Mind and body connection 4.1, 6.1, 8.1, 11.2, 12.6, 15.2, 16.2

Self-compassion Encouraging a positive self-identity 11.2, 13.1, 13.2, 13.4, 13.5

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Intervention Model Description:
Randomized controlled waitlist (20 experimental and 20 waitlist)Randomized controlled waitlist (20 experimental and 20 waitlist)
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Preliminary Randomised Controlled Study Online Mindfulness-Based-Cognitive-Intervention for African Caribbean Men
Anticipated Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Dec 15, 2022
Anticipated Study Completion Date :
Dec 23, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental Randomized controlled waitlist

n=20 (will receive Mindfulness-based cognitive intervention)

Behavioral: Mindfulness based cognitive intervention based on the behavioural change techniques taxonomy
An online mindfulness-based cognitive intervention is used as a proposed treatment intervention for erectile dysfunction among African- Caribbean men based in the United Kingdom.

Other: Waitlist Randomized controlled waitlist

waitlist Randomized controlled waitlist n=20 (will not receive Mindfulness-based cognitive intervention for 1 month)

Behavioral: Mindfulness based cognitive intervention based on the behavioural change techniques taxonomy
An online mindfulness-based cognitive intervention is used as a proposed treatment intervention for erectile dysfunction among African- Caribbean men based in the United Kingdom.

Outcome Measures

Primary Outcome Measures

  1. Change in baseline in erectile dysfunction on a 15 item questionnaire at 4,8 and 12 weeks [0 baseline 4, 8 and 12 week measurements]

    This consists of 15 questions with 6 response categories measuring erectile functioning, satisfaction and desire for the last 4 weeks. Cronbach alpha= 0.82 to 0.93. The response categories range from 0=no sexual activity to 5=almost always/always. Subscale scoring is divided into 5 areas including sexual activity, sexual intercourse, sexual stimulation, sexual, ejaculation and orgasm. There is no reverse scoring where scores range from 0 to 75, the latter being higher levels of erectile functioning.

  2. Change in baseline in mindfulness on a 15 item questionnaire at 4,8,and 12 weeks [0 baseline 4, 8 and 12 week measurements]

    This is a 15-item questionnaire which consists of 5 response categories (1=never or rarely true through to 5= very often/always true). Cronbach's alpha ranges between 0.69-0.76. There are 7 reversed items. Subscale scoring is divided into 5 areas including observing, describing, acting with awareness, non-judging and non-reactivity. Higher scores reflect higher levels of mindfulness endorsement.

  3. Change in baseline in wellbeing on a 7 item questionnaire at 4, 8 and 12 weeks [0 baseline, 4, 8 and 12 week measurements]

    A positively worded 7 item questionnaire with 5 response categories looking at functioning and feeling aspects of well-being. The response categories include 1=none of the time to 5=all of the time. Cronbach alpha- 0.89-0.91. There is no reverse scoring. Scores range from 7 to 35 where the latter is the highest level of wellbeing.

  4. Change in baseline in sexual self-efficacy on a 25 item questionnaire at 4, 8 and 12 weeks [0 baseline, 4, 8 and 12 week measurements]

    The Sexual Self-Efficacy Erectile tool is a 25-item questionnaire which focuses on sexual confidence and behaviour change associated with therapy. Participants responses are measured via a 10-item scale ranging from 10 to 100. Here, 10 is the lowest level of self-efficacy and 100 is the highest. There are no reverse questions. The Cronbach's alpha for men with erectile difficulties is α =0.88 (high) and for men without erectile difficulties, α =0.62 (low to moderate).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • African Caribbean men with erectile dysfunction

  • Aged 18 years and above

  • Registered with a general practitioner

Exclusion Criteria:
  • Taking Viagra during the study

  • Aged younger than 18 years

  • Non-African-Caribbean

  • Not registered with a general practitioner

Contacts and Locations

Locations

Site City State Country Postal Code
1 London Met university London United Kingdom N7 8DB

Sponsors and Collaborators

  • London Metropolitan University

Investigators

  • Principal Investigator: Samantha Banbury, PhD, Reader

Study Documents (Full-Text)

More Information

Publications

Responsible Party:
Samantha Banbury, Principal Investigator, London Metropolitan University
ClinicalTrials.gov Identifier:
NCT05167955
Other Study ID Numbers:
  • LondonMU
First Posted:
Dec 22, 2021
Last Update Posted:
Feb 15, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Samantha Banbury, Principal Investigator, London Metropolitan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 15, 2022